Antifungal compounds and methods of use

ABSTRACT

The invention provides screening methods for detecting and identifying compounds that bind to fungal specific target proteins and nucleic acids, as well as compounds which, upon binding or otherwise interacting with the target protein, can inhibit fungal growth, a method of preventing or inhibiting fungal growth in culture, a method of preventing or inhibiting fungal growth in a mammal and a method of studying pathogenic mycetes using such nucleic acid and/or protein sequences. Particularly preferred is the inhibition of the fungus  Candida albicans.

PRIORITY

[0001] This application claims priority under 35 U.S.C. § 119 from Provisional Patent Application Serial No. 60/215,164, filed Jun. 29, 2000, and Provisional Patent Application Serial No. 60/224,457, filed Aug. 10, 2000, which are hereby incorporated by reference in their entireties.

FIELD OF THE INVENTION

[0002] The invention encompasses the use of fungal cidal targets in the screening for, isolation and development of antifungal chemicals and drugs to be used in the treatment of fungal infections, such as infections with Candida albicans. The invention encompasses methods of determining fungal cidal targets. Such fungal cidal targets are encompassed by nucleic acid and protein sequences encoded by such nucleic acid sequences which are isolated from S. ceriviseae, shown to be present in other fungi such as Candida albicans, and are shown to be both essential and fungal specific in both Sacchromyces ceriviseae and Candida albicans. The essential fungal specific nucleic acid and protein sequences may also be used in studying pathogenic mycetes or fungi.

BACKGROUND OF THE INVENTION

[0003] Fungi are a distinct class of microorganisms, of which most are free-living. They are eukaryotic organisms containing a nuclear membrane, mitochondria and endoplasmic reticulum. In addition, they are non-motile, do not contain chlorophyl and develop from spores (i.e. yeasts, molds, mushrooms and rusts). The cell structure usually includes a rigid cell wall of mannan, glucan and chitin and a cytoplasmic membrane with a large percentage of ergosterol. The size and morphology of fungi vary from monomorphic yeasts like Cryptococcus and Saccharomyces species and dimorphic fungi like Candida albicans to filamentous fungi like Aspergillus species.

[0004] In contrast to bacteria, which are generally considered mammalian pathogens, fungi tend to be plant pathogens. However, in addition to the well recognized group of dermatophytes (e.g. cause of “athlete's foot”), an increasingly large group of fungi turn out to be able to act as opportunistic human pathogens producing disease only in compromised individuals. As the result of an aging population as well as an increase in the number of immunocompromised patients, e.g., patients with acquired immunodeficiency syndrome (AIDS), patients undergoing cancer chemotherapy, or immunosuppressive therapy (e.g. treatment with corticosteroids) and patients undergoing organ transplantation, the incidence of fungal infections is increasing rapidly.

[0005] Fungi parasitize many different tissues. Most infections begin by colonization of the skin, a mucosal membrane or the respiratory epithelium. Superficial fungi and subcutaneous pathogens cause indolent lesions of the skin. Passage through the initial surface barrier is accomplished through a mechanical break in the epithelium. Although most fungi are readily killed by neutrophils, some species are resistant to phagocytic killing and can infect otherwise healthy individuals. The most virulent fungi cause systemic infections, a progressive disease leading to deep seated visceral infections in otherwise healthy individuals (see e.g. Sherris Medical Microbiology, Third Edition, Kenneth J. Ryan, ed., Appleton & Lange, Norwalk, Conn., 1994).

[0006] The major fungal pathogens in North America are Histoplasma capsulatum, Coccidioides immitis, Blastomyces dermatitidis, Cryptococcus neofonnans, Candida species, such as but not limited to Candida albicans and Aspergillus species (Medically Important Fungi, Second Edition, Davise H. Larone, Ed., American Society for Microbiology, Washington, D.C.). The yeast C. albicans (C. albicans) is one of the most pervasive fungal pathogens in humans. It is the cause of an increasing financial and logistic burden on the medical care system and its providers due to its ability to opportunistically infect a diverse spectrum of immunocompromised hosts, which are a quickly growing population of patients in today's society. Although C. albicans is a member of the normal flora of the mucous membranes in the respiratory, gastrointestinal, and female genital tracts, it may gain dominance in such locations (e.g. upon treatment with antibacterial antibiotics, in patients with diabetes or in patients using corticosteroids) and be associated with pathologic conditions. In addition, almost all HIV-positive individuals suffer from a Candida infection prior to the onset of developing full-blown AIDS.

[0007] Sometimes C. albicans produces progressive systemic disease, particularly if cell-mediated immunity is impaired. In 1994, about thirty percent of patients suffering from leukemia or undergoing organ transplants developed a systemic Candida infection of which thirty percent have been estimated to have succumbed to the infection.

[0008] Only a handful of agents are active against fungi. For life threatening disease caused by any of the pathogenic fungi, amphotericin B is the agent of choice. This drug, however, is associated with numerous severe side effects such as fever, dyspnea and tachycardia, and dosage is limited over the lifetime of the patient because of renal toxicity. An agent frequently used concurrently is flucytosine, a nucleoside analog, which cannot be used independently of other agents because of the rapid appearance of resistance. Untoward effects of treatment with flucytosine include leukopenia, thrombocytopenia, rash, nausea, vomiting, diarrhea, and severe enterocolitis.

[0009] In conditions where the patient's life is not threatened, ketoconazole can be used as a long-term therapy for blastomycosis, histoplasmosis, or coccidioidomycosis. Fluconazole also has a significant role in the treatment of superficial fungal infections. Both compounds are from the same class, the triazoles, and are cytostatic. The emergence of resistance and hepatic toxicity limits the use of triazoles such as fluconazole and ketoconazole. The newest triazole, itraconazole, has similar pharmacokinetics and spectrum of activity as fluconazole. None of the azoles can be used for life threatening or deep seated fungal infections. They are only effective in reducing colonization of fungi such as Candida species and for treating superficial mycoses.

[0010] All major antifungal agents function by attacking, either directly or indirectly, ergosterol, a component of the cell wall. Amphotericin B and other polyene macrolide compounds like nystatin interact with ergosterol in the cell membrane and form pores or channels that increase the permeability of the membrane. Resistance to amphotericin B in mutant strains is accompanied by decreased concentrations of ergosterol in their cell membranes. Imidazoles and triazoles inhibit sterol 14-″-demethylase, a microsomal cytochrome P₄₅₀-dependent enzyme system. Imidazoles and triazoles thus impair the biosynthesis of ergosterol for the cytoplasmic membrane, leading to the accumulation of 14-″-methyl sterols, which impair certain membrane-bound enzyme systems (see, The Pharmacological Basis of Therapeutics, Eighth Edition, Goodman and Gilman, Pergamon Press, 1990).

[0011] Nystatin, amphotericin B, flucytosine and the various azoles have all been used to treat oral and systemic Candida infections. However, orally administered nystatin is limited to treatment within the gut and is not applicable to systemic treatment, and resistance to flucytosine is so widespread that it is only used in combination with other drugs. Some life-threatening systemic infections are susceptible to treatment with the azoles or amphotericin B. Azoles have been the most successful drugs used for treatment of such infections in the last few years but they work relatively slowly, have to be taken for months, and are fungistatic rather than fungicidal. While such azole antifungal agents exhibit significantly lower toxicity compared to amphotericin B, their mechanism of action and inactivation of cytochrome P₄₅₀ prosthetic groups in certain enzymes preclude their use in patients that are simultaneously receiving other drugs that are metabolized by the body's cytochrome P₄₅₀ enzymes.

[0012] Widespread use of azoles has also resulted in an important change in the spectrum of Candida infections. Whereas C. albicans used to be the common cause of Candidosis, 50% of these infections are now caused by non-albicans species which tend to be less susceptible to azole treatment. In addition, a quickly rising percentage of C. albicans isolates obtained from infected patients have been found to be resistant to azoles.

[0013] There is thus an immediate need for an effective treatment of opportunistic infections caused by C. albicans and other fungi. Although the majority of life-threatening fungal infections are caused by C. albicans, infections caused by other less common fungi as discussed above, e.g., Aspergillus fumigatus have a worse prognosis. In large part this is due to the absence of diagnosis until a very late stage of infection, usually post-mortem. Therefore it is desirable that novel compounds be able to act against all pathogenic fungi, preventing the need for precise, time-consuming diagnosis.

[0014] Development of an effective method and composition for treatment of fungal infections is a critical goal of the pharmaceutical industry. The industry has made numerous efforts to identify fungal-specific drugs, with only limited success. It would be of great value to identify a new class of antifungal drugs that block a fungal target other than ergosterol. This target should be fungal-specific and should lead to development of a drug that is effective in preventing or inhibiting the growth of, and preferentially killing, the organisms that are resistant to current therapy.

[0015] Antifungal drug development often relies on the screening of a large number of compounds before one or more lead compounds are found that are effective against the target fungi. Thus, it is critical for the development of these screens to define proteins essential for survival or growth of the target fungi and to discover means of purifying or producing such proteins. Therefore, there is a need in the art to identify essential fungal structural or functional elements that can serve as targets for drug intervention, and for methods and compositions for identifying useful anti-fungal agents that interact with or inhibit essential fungal elements that can be used to treat fungal infections by preventing or inhibiting the growth of, and preferentially killing, the fungi.

SUMMARY OF THE INVENTION

[0016] The present invention is based on the determination of Saccharomyces cerevisiae proteins which are potential targets to kill S. cerevisiae cells. The invention provides a screening method for detecting and identifying a compound that binds to a homologous target protein isolated from C. albicans, as well as compounds which can inhibit C. albicans and other fungal growth. The invention also provides a method for evaluating the toxicity of such a fungal inhibitor in mammalian cells.

[0017] The invention utilizes target proteins involved in such processes as DNA synthesis, DNA replication, DNA transcription, mRNA translation, post-translational modification of proteins, and intracellular transport of proteins, as well as target proteins whose exact cellular functions are unknown. In preferred embodiments, the invention provides for the use of S. cerevisiae target proteins listed in Table 1 together with C. albicans and human homologs, depicted therein by their respective amino acid sequences which are provided in FIG. 79. The nucleic acid sequences corresponding to these amino acid sequences are depicted in FIG. 80.

[0018] Each of the S. cerevisiae DNA sequences, and their predicted target protein sequences, which are utilized in practicing the invention are publicly available. The essentiality of each of such S. cerevisiae genes may already be known or may be determined and/or corroborated through the analysis of the ability to knock out the gene's function in S. cerevisiae. The present invention thus provides a method of determining and/or validating the essentiality of the S. ceriviseae gene and the target protein encoded by that gene. More specifically, the invention is directed to the determination of the S. ceriviseae protein as a cidal target to be used in the determination and isolation of a homologous target in C. albicans. The C. albicans target may then be used in the screening of compounds which can inhibit Candida albicans and other fungal growth.

[0019] Following the determination of the essentiality of the S. cerevisiae gene, the S. ceriviseae DNA sequence may be used to isolate a homologous fungal gene. Thus, in another aspect, the invention is based on the determination of a C. albicans nucleic acid encoding the C. albicans protein as a target which is essential for the growth of C. albicans.

[0020] In a still further aspect, the invention provides for producing a recombinant target C. albicans target protein, comprising culturing a host cell transformed with a nucleic acid encoding the C. albicans target protein under conditions sufficient to permit expression of the nucleic acid encoding the C. albicans target protein and isolating the C. albicans target protein to be used in assays described below.

[0021] Sequence alignments utilizing the S. cerevisiae nucleic acid or protein sequences and/or the C. albicans nucleic acid or protein sequences in combination with known sequences available in Genbank may be carried out in order to demonstrate any similarity or differences between different fungi, i.e., S. cerevisiae, C. albicans, and Aspergillus, and mammals. In this manner, homologous genes can be isolated. One example of such analysis would be BLAST™ analysis.

[0022] In a further embodiment, following the determination that the target protein in Saccharomyces cerevisiae is a cidal target, and that the homologous protein in Candida albicans is essential for growth, the C. albicans protein may be used as a target to isolate candidate inhibitors of fungal growth and/or infection. Detection and identification of compounds that bind to the essential protein may be performed in the presence of a plurality of candidate inhibitor compounds. In carrying out the screening methods of the invention which involve screening a plurality of candidate inhibitor compounds, the plurality of inhibitor compounds may be screened together in a single assay or individually using multiple simultaneous individual detecting steps.

[0023] In another aspect, the invention provides a method of preventing or inhibiting fungal, particularly C. albicans, growth in culture, by contacting the culture with an inhibitor compound that selectively inhibits the biological activity of a fungal target protein, particularly a C. albicans target protein.

[0024] In a further aspect, the invention provides a method of preventing or inhibiting fungal, particularly C. albicans, growth in a mammal, comprising administering to the mammal an effective amount of an inhibitor compound that selectively inhibits the biological activity of a fungal, particularly C. albicans, target protein.

[0025] In a still further aspect, the invention provides a method of preventing or inhibiting fungal, particularly C. albicans, growth in a mammal, comprising administering to the mammal an effective amount of an inhibitor compound, wherein the inhibitor selectively inhibits the biological activity of a fungal, particularly C. albicans, target protein, but inhibits the biological activity of the homologous mammalian protein to a lesser degree, or not at all.

[0026] In yet another aspect, the invention provides a method of preventing or inhibiting fungal growth, comprising administering to a fungal infection an effective amount of an inhibitor compound that selectively inhibits the biological activity of a fungal target protein.

[0027] In still another aspect, the invention provides a method of studying pathogenic mycetes using such nucleic acid and/or protein sequences.

[0028] Other features and advantages of the invention will be apparent from the description, preferred embodiments thereof, the drawings, and from the claims. TABLE 1 Preferred target proteins S. cerevisiae C. albicans Human Gene name ORF name¹ Sequence Sequence Sequence Genbank Acc#² RPC34 YNR003C SEQ ID NO: 1 SEQ ID NO: 2 SEQ ID NO: 3 U93869 POP3 YNL282W SEQ ID NO: 4 SEQ ID NO: 5 — n/a TFA2 YKR062W SEQ ID NO: 6 SEQ ID NO: 7 SEQ ID NO: 8 NP_002086 NAB2 YGL122C SEQ ID NO: 9 SEQ ID NO: 10 SEQ ID NO: 11 AAD42873 MPT1 YMR005W SEQ ID NO: 12 SEQ ID NO: 13 SEQ ID NO: 14 CAA72189 MTR2 YKL186C SEQ ID NO: 15 SEQ ID NO: 16 — n/a BOS1 YLR078C SEQ ID NO: 17 SEQ ID NO: 18 SEQ ID NO: 19 NP_003560 POL30 YBR088C SEQ ID NO: 20 SEQ ID NO: 21 SEQ ID NO: 22 P12004 RSA2 YMR131C SEQ ID NO: 23 SEQ ID NO: 24 SEQ ID NO: 25 NP_005601 SQT1 YIR012W SEQ ID NO: 26 SEQ ID NO: 27 SEQ ID NO: 28 NP_001078 MTW1 YAL034W-A SEQ ID NO: 29 SEQ ID NO: 30 — n/a TFB1 YDR311W SEQ ID NO: 31 SEQ ID NO: 32 SEQ ID NO: 33 W19128 SPC98 YNL126W SEQ ID NO: 34 SEQ ID NO: 35 SEQ ID NO: 36 AAC39727 BFR2 YDR299W SEQ ID NO: 37 SEQ ID NO: 38 SEQ ID NO: 39 NM_000055 RNA1 YMR235C SEQ ID NO: 40 SEQ ID NO: 41 SEQ ID NO: 42 CAA57714 GCD7 YLR291C SEQ ID NO: 43 SEQ ID NO: 44 SEQ ID NO: 45 AAC42002 SK16 YGR195W SEQ ID NO: 46 SEQ ID NO: 47 SEQ ID NO: 48 BAA91279 NIP1 YMR309C SEQ ID NO: 49 SEQ ID NO: 50 SEQ ID NO: 51 AAD03462 LCP5 YER127W SEQ ID NO: 52 SEQ ID NO: 53 SEQ ID NO: 54 AL050003 NCE103 YNL036W SEQ ID NO: 55 SEQ ID NO: 56 — n/a ECO1 YFR027W SEQ ID NO: 57 SEQ ID NO: 58 — n/a ORC2 YBR060C SEQ ID NO: 59 SEQ ID NO: 60 SEQ ID NO: 61 Q13416 CNS1 YBR155W SEQ ID NO: 62 SEQ ID NO: 63 SEQ ID NO: 64 NP_004614 YPD1 YDL235C SEQ ID NO: 65 SEQ ID NO: 66 SEQ ID NO: 67 CAA78727 TIM10 YHR005C-A SEQ ID NO: 68 SEQ ID NO: 69 SEQ ID NO: 70 NP_036588 SRB4 YER022W SEQ ID NO: 71 SEQ ID NO: 72 SEQ ID NO: 73 BAA88763

BRIEF DESCRIPTION OF THE DRAWINGS

[0029] FIGS. 1-26 provide sequence alignments and identity determinations for the target proteins presented herein. Each figure refers to one target protein as identified in Table 2, comparing amino acid sequences from S. cerevisiae, C. albicans, and, if available, human homologs. Sequence alignment was carried out using Clustal W (Thompson et al., Nucleic Acids Res. 1994;22:4673-80), and percentage identities determined using the Genetics Computer Group (“GCG”) GAP Program (Madison, Wis.) with a gap creation penalty of 12 and a gap extension penalty of 4.

[0030] FIGS. 27-52 provide S. cerevisiae inactivation analyses of the target genes/proteins identified in Table 1. These data show the essentiality of each gene for S. cerevisiae growth. Each figure refers to one target protein. Inactivation analyses were conducted by placing the S. cerevisiae expression of a target gene under the control of a metal-sensitive element and incubating the yeast cells together with a Cu-salt, as described in the Detailed Description below and in Example 1.

[0031] FIGS. 53-78, A and B for each, provide C. albicans deletion analyses of the target genes/proteins identified in Table 1. These data indicate the essentiality of each gene for C. albicans growth. Each figure refers to one target protein. Deletion analyses were conducted as described in the Detailed Description, and C. albicans transformation as described in Example 2 below.

[0032]FIG. 79 provides amino acid sequences for each of the proteins disclosed herein and depicted in Table 1.

[0033]FIG. 80 provides nucleic acid sequences corresponding to each of the proteins disclosed in FIG. 79.

DETAILED DESCRIPTION OF THE INVENTION

[0034] All patent applications, patents, and literature references cited in this specification are hereby incorporated by reference in their entirety.

[0035] This invention is directed to essential fungal proteins isolated from S. cerevisiae to be used in the determination and/or isolation of a homologous protein from fungi, particularly C. albicans. These fungal proteins, each of which described in more detail below, play essential roles in cell viability and/or growth, and are conserved among fungi. Because these fungal proteins are essential for viability and/or growth of fungal cells, a compound that blocks the biological activity of such a target protein would be expected to have fungicidal and/or fungistatic properties. Since amino acid sequences of any such protein from different fungal sources are likely to be more similar to one another than to the corresponding human protein, it is expected that certain compounds that bind to the fungal protein will not bind to the corresponding human protein, and so will be specific inhibitors of fungal cell growth. Therefore, the invention is also directed to assays to screen for inhibitors of these target proteins which are active against fungi.

[0036] In general, nucleic acid manipulations and other related techniques used in practicing the present invention employ methods that are well known in the art, as disclosed in, e.g., Molecular Cloning, A Laboratory Manual (2nd Ed., Sambrook, Fritsch and Maniatis, Cold Spring Harbor) and Current Protocols in Molecular Biology (Eds. Ausubel, Brent, Kingston, More, Feidman, Smith and Stuhl, Greene Publ. Assoc., Wiley-Interscience, NY, N.Y., 1997).

Definitions

[0037] 1. The terms “Prevention” and “Inhibition” as used herein may be used interchangeably. “Inhibition” as used herein refers to a reduction in the parameter being measured, whether it be fungal growth, DNA transcription, or another parameter related to a selected process relating to the biological activity of a target protein. The amount of such reduction is measured relative to a standard (control). Because of the multiple interactions of various fungal protein in cell division, growth regulation, cell cycle regulation, and other growth and/or metabolic processes, the amount of target product needed to produce a detectable inhibition will vary with respect to the particular screening assay employed. “Reduction” is defined herein as a decrease of at least 25% relative to a control, preferably of at least 50%, and most preferably of at least 75%.

[0038] 2. “Growth” or “multiplication” as used herein refers to the normal growth pattern of fungi, particularly S. cerevisiae and/or C. albicans, i. e., to a cell doubling time of 60-90 minutes during the log phase of growth. In rich media, wild-type S. cerevisiae strains have a doubling time of 90 minutes, while wild type C. albicans doubling time is closer to approximately 60 minutes. Growth of the cells may be measured by following the optical density of cells in liquid media. An increasing optical density indicates growth. Growth can also be measured by colony formation from single cells on solid media plates.

[0039] 3. “Viability” as used herein refers to the ability of the S. cerevisiae or C. albicans cells to resume growth following a treatment of the cells which results in cessation of growth. Examples of such treatments resulting in cessation of growth include, but are not limited to, transient inactivation of a gene product required for growth or treatment with an antifungal drug. One typical means by which viability is measured is by testing the ability of cells to form colonies on solid media plates following removal of the treatment which resulted in a cessation of growth. Cells that fail to form colonies are considered inviable.

[0040] 4. “Cidal” as used herein is defined as a rapid loss in viability. Rapid is defined as a population of cells losing viability with a measured half-life of at least about 2 hours or less.

[0041] 5. A “homologous” protein as used herein is defined as any protein which possesses a protein domain with at least about 30% sequence identity or similarity to a given protein, preferably at least about 40% sequence identity, and most preferably at least about 50% sequence identity. Useful sequence comparison algorithms to determine degree of sequence similarity include BLAST™, FASTA, DNA Strider, the GCG pileup program (Wisconsin Package version 10, Genetics Computer Group, Madison, Wis.), as well as alignment schemes such as Clustal W (See Thompson et al., supra), using, e.g., the default parameters provided with these algorithms. Sequences that are substantially homologous can be identified by comparing the sequences using standard software available in sequence data banks, or in a Southern hybridization experiment under, for example, stringent conditions as defined for that particular system. (See “hybridization”, below)

[0042] 6. A “protein domain” as used herein is defined as a region of a protein which is at least about 50 amino acids ranging to the full length of the protein.

[0043] 7. “Biological activity” as used herein refers to the ability of a protein to promote or sustain cell growth and/or metabolism through a known or unknown cellular mechanism. Biological activity need not be measured in living cells; an in vitro system consisting of the protein together with other chosen components, designed to reflect the ability of the protein to promote or sustain cell growth and/or metabolism, may also be used to evaluate biological activity.

[0044] 8. “Target protein” or “cidal protein” as used herein refers to an essential protein involved in, e.g., growth and/or metabolism. Inhibition of the biological activity of a fungal target protein results in an inhibition of fungal growth. Target proteins may play essential roles in processes which include, but are not limited to, DNA synthesis, DNA repair, transcription, mRNA transport, mRNA processing, translation, protein transport, protein processing, cell cycle control, cell division, and cell signaling. The term “target protein” also includes fragments and polypeptides, as well as target proteins modified by any means known in the art, e.g., by radiolabeling, conjugation, mutations in amino acid sequence, using chemically modified amino acid residues in the target protein, and so forth.

[0045] 9. “Mycete” or “fungi” as used herein refers to a eukaryotic organism which carries spores, nutrition of which takes place via absorption, which is deficient in chlorophyll and which reproduces sexually or asexually.

[0046] 10. “Nucleic acid” or “polynucleotide” as used herein refers to purine- and pyrimidine-containing polymers of any length, either polyribonucleotides or polydeoxyribonucleotides or mixed polyribo-polydeoxyribo nucleotides. This includes single- and double-stranded molecules, i.e., DNA-DNA, DNA-RNA and RNA-RNA hybrids, as well as “protein nucleic acids” (PNA) formed by conjugating bases to an amino acid backbone. This also includes nucleic acids containing modified bases.

[0047] 11. An “isolated” nucleic acid or polypeptide as used herein refers to a nucleic acid or polypeptide that is removed from its original environment (for example, its natural environment if it is naturally occurring). An isolated nucleic acid or polypeptide contains less than about 50%, preferably less than about 75%, and most preferably less than about 90%, of the cellular components with which it was originally associated.

[0048] 12. A nucleic acid or polypeptide sequence that is “derived from” a designated sequence refers to a sequence that is related in nucleotide or amino acid sequence to a region of the designated sequence. For nucleic acid sequences, this encompasses sequences that are homologous or complementary to the sequence, as well as “sequence-conservative variants” and “function-conservative variants.” For polypeptide sequences, this encompasses “function-conservative variants.” Sequence-conservative variants are those in which a change of one or more nucleotides in a given codon position results in no alteration in the amino acid encoded at that position. Function-conservative variants are those in which a given amino acid residue in a polypeptide has been changed without altering the overall conformation and function of the native polypeptide, including, but not limited to, replacement of an amino acid with one having similar physical and/or chemical properties (such as, for example, acidic, basic, hydrophobic, and the like). “Function-conservative” variants of a designated polypeptide also include any polypeptides that have the ability to elicit antibodies specific to the designated polypeptide.

[0049] 13. Nucleic acids are “hybridizable” to each other when at least one strand of nucleic acid can anneal to another nucleic acid strand under defined stringency conditions. Stringency of hybridization is determined, e.g., by a) the temperature at which hybridization and/or washing is performed, and b) the ionic strength and polarity (e.g., formamide concentration) of the hybridization and washing solutions, as well as other parameters. Hybridization requires that the two nucleic acids contain substantially complementary sequences; depending on the stringency of hybridization, however, mismatches may be tolerated. The appropriate stringency for hybridizing nucleic acids depends on the length of the nucleic acids and the degree of complementarity, variables well known in the art.

[0050] Hybridizable polynucleotides may be of any length. In one embodiment, such polynucleotides are at least 7, preferably at least 25 and most preferably at least 100 nucleotides long. In another embodiment, the polynucleotide that hybridizes to any of the polynucleotides of the invention is of the same length as the polynucleotide of the invention. Nucleic acids that are hybridizable to other nucleic acids are capable of hybridizing with their complements under the hybridization conditions defined herein as “high stringency” as defined below.

[0051] Prehybridization treatment of the support (nitrocellulose filter or nylon membrane), to which is bound the nucleic acid capable of being hybridized at 65EC for 6 hours with a solution having the following composition: 4×SSC, 10×Denhardt (1× Denhardt is 1% Ficoll, 1% polyvinylpyrrolidone, 1% BSA (bovine serum albumin); 1×SSC consists of 0.15M of NaCl and 0.015M of sodium citrate, pH 7);

[0052] Replacement of the pre-hybridization solution in contact with the support by a buffer solution having the following composition: 4×SSC, 1×Denhardt, 25 mM NaPO₄, pH 7, 2 mM EDTA, 0.5% SDS, 100 g/mL of sonicated salmon sperm DNA containing a nucleic acid probe, in particular as radioactive probe, and previously denatured by a treatment at 100EC for 3 minutes;

[0053] Incubation for 12 hours at 65EC;

[0054] Successive washings with the following solutions: (i) four washings with 2×SSC, 1×Denhardt, 0.5% SDS for 45 minutes at 65EC; (ii) two washings with 0.2×SSC, 0.1×SSC for 45 minutes at 65EC; and (iii) 0.1×SSC, 0.1% SDS for 45 minutes at 65EC.

[0055] 14. A “promoter sequence” as used herein is defined as a DNA regulatory region capable of binding RNA polymerase in a cell and initiating transcription of a downstream (3′ direction) coding sequence.

[0056] 15. A “candidate inhibitor,” as used herein, is any compound with a potential to inhibit Candida albicans or other fungal growth and/or metabolism via an activity mediated by any of the target proteins described in Table 1, and throughout the specification.

[0057] 16. “ATLAS”, an abbreviation of “Any Target Ligand Assisted Screening” as used herein refers to the screening method described in the section entitled “Primary Inhibitor Screening; High-Throughput Methods for Screening Inhibitors.”

Target proteins

[0058] The present invention is based on the isolation of DNA encoding fungal proteins involved in cellular growth and/or metabolism, particularly those derived from the S. cerevisiae and/or Candida albicans genes listed in Table 1, and the determination of the essentiality and or cidality of such fungal gene. The discovery and characterization of these S. cerevisiae target proteins and/or their C. albicans homologs, and the elucidation of differences between the fungal and mammalian target proteins, implicates these protein, particularly the C. albicans protein, as an important target for the development of new methods and compositions for the treatment of fungal infections. Agents which selectively interfere the biological activity would likely be candidates for anti-fungal, particularly anti-C. albicans and related fungi, therapeutics. The present invention also encompasses methods for identifying compounds that selectively interfere with C. albicans target protein activity and thus may comprise useful antifungal agents.

[0059] Ideally, an antifungal compound directs its action against a target that is present in fungi but absent in human cells. Such targets, however, are important for cell function and tend to be conserved in evolution and, thus, be present in both human and fungal cells. In such cases, the target protein is present in both cell types, as noted above, but the human homolog of the target protein has an amino acid sequence that distinguishes it from the fungal target protein.

[0060] If a human homolog of the target protein has been identified, such a human sequence is considered distinguishable from the fungal sequence if it has less than about 50%, preferably less than about 40%, and even more preferably less than about 30% sequence identity. The lower the sequence similarity, the higher the chance for identifying compounds that act specifically against the fungal target protein but not its human homolog. However, an important factor is also the sequence similarity between different fungal homologs of the target protein. If homologous proteins derived from two different fungal sources such as, e.g., S. cerevisiae and C. albicans, display a high sequence similarity such as, e.g., higher than 50%, more preferably 70%, and even more preferably higher than 90%, this allows for a higher chance of identifying an inhibitor specific for the fungal target proteins but not their human homolog. Thus, a higher than optimal sequence similarity between the fungal and human target protein homologs does not preclude finding a substance which only inhibits the biological activity of the fungal protein.

[0061] Each preferred target protein is described below. Non-limiting examples of some assays for some of the target proteins are also provided. Such assays are useful in identifying and/or measuring the biological activity of target proteins, e.g., in the presence of a potentially inhibitory compound. Amino acid sequences for each target protein in S. cerevisiae, C. albicans, and, where relevant, human, can be found in Table 1. Sequence identity determinations between the the S. cerevisiae, C. albicans, and, if available, human homologs, are provided in Table 2.

RPC34

[0062] RPC34 (C34) is an essential and specific subunit of RNA polymerase III complex (Stettler, S., et al., J. Biol. Chem., 1992; 267:21390-21395). RNA polymerase III is responsible for transcription of tRNAs, 5S rRNA, and some other small RNAs. Three RNA polymerase III unique subunits, C34, C82, and C31 form a complex that interacts with 70-kDa component of transcription factor TFIIIB via C34 (Werner, M., et al., J. Biol. Chem., 1993; 268:20721-20724). C34 subunit is a major determinant of pol III recruitment by pre-initiation complex. Interaction between C34 and TFIIIB70 is essential for pre-initiation complex formation and later during promoter opening (Brun, I., et al., EMBO J., 1997; 16:5730-5741). It has been demonstrated that strains carrying temperature-sensitive or cold-sensitive mutations in RPC34 are impaired in tRNA synthesis (Stettler, S., et al., J. Biol. Chem., 1992; 267:21390-21395; Brun, I., et al., EMBO J., 1997; 16:5730-5741). RPC39 human homolog of RPC34 has been identified (Wang, Z. and Roeder, R. Gen. Dev., 1997; 11:327-7949). RPC34 and RPC39 are 27% identical and 50% similar.

[0063] RPC34 assays:

[0064] (a) ATLAS

[0065] (b) Cell-based assays in S. cerevisiae and human cells were developed utilizing the information that in the absence/inability to perform, the function of RPC34 tRNA synthesis decreases (Stettler, S., et al., J. Biol. Chem., 1992; 267:21390-21395; Brun, I., et al., EMBO J., 1997; 16:5730-5741). If the compound specifically binds to Rpc34p, a tRNA level decrease can be detected after addition of the compound to the growing media. Similar assay in human cells can be designed based on the same principle. The level of tRNA can be assayed upon addition of a compound to the cells at different time points.

[0066] (c) In vitro assays can be developed using purified RNA polymerase III transcription factors, including RPC34, to assess tRNA and 5S rRNA levels in the presence/absence of a compound (Kassavetis, G., et al., EMBO J., 1999; 18:5042-5051).

[0067] (d) A reporter-based assay can be developed utilizing a two-hybrid system, knowing that RPC34 physically interacts with C82, C31, and TFIIIB70. One of the proteins can be fused with a transcriptional activator and the other with a DNA-binding protein. The ability of the two proteins to interact with each other in the presence or absence of a compound can be measured by monitoring enzymatic activity of a reporter gene expressed from the promoter.

POP3

[0068]Saccharomyces cerevisiae POP3 is involved in post-transcriptional processing of the large precursor RNAs into the mature functional forms of tRNA and rRNA (Dichtl, B. and D. Tollervey, EMBO Journal, 1997; 16:417-429; Chamberlain, J. R., et al., Genes and Development, 1998; 12:1678-1690). This processing of tRNA and rRNA is carried out by the RNase MRP and RNase P ribonucleoproteins, respectively, but the two complexes are known to have extensive subunit overlap (Chamberlain, J. R., et al., Genes and Development, 1998; 12:1678-1690). Mutations in POP3 result in phenotypes identical to loss of RNase MRP, including interference with the complete processing of tRNA and rRNA (Dichtl, B. and D. Tollervey, EMBO Journal, 1997; 16:417-429; Chamberlain, J. R., et al., Genes and Development, 1998; 12:1678-1690). POP3 is essential for cell growth in Saccharomyces cerevisiae (Dichtl, B. and D. Tollervey, EMBO Journal, 1997; 16:417-429).

[0069] POP3 Assays:

[0070] (a) ATLAS: CaPop3 protein could be purified and challenged with an environmental condition, such as higher temperature or reduced pH, that unfolds the protein. A compound that binds to CaPop3 protein may stabilize the native conformation of the protein.

[0071] (b) Two hybrid interruption screen using another interacting protein: CaPOP3 and a Candida albicans ortholog of another subunit of either the RNase MRP or the RNase P complex could be placed into yeast two-hybrid screening vectors, one as the bait and one as the target. Binding by the two proteins will induce expression of a reporter gene. A compound that interferes in the binding of the two proteins should disrupt the induction of the reporter gene, allowing such compounds to be identified in a screening format. Interacting proteins other than those in the RNase MRP or RNase P complex could be used in this format.

TFA2

[0072]Saccharomyces cerevisiae TFA2 is a subunit of the general RNA polymerase II transcription initiation factor, TFIIE. The gene product of TFA2 forms a hetero-tetramer with that of TFA1, and both genes are essential for cell viability (Feaver et al., J Biol Chem, 1994, 269:27549-53). The genes for TFA1 and TFA2 were identified from the purified protein shown to have an activity required for accurately initiated transcription from promoters in vitro, and the gene sequences have significant homology to mammalian TFIIE (Feaver et al., J Biol Chem, 1994, 269:27549-53). The requirement for TFIIE to carry out transcription of a gene varies, depending on the promoter structures, (Sakur et al., J Biol Chem, 1997, 272: 15936-15942). It has been suggested that yeast GAL11 product enhances the interaction between TFIIE and the RNA polymerase II holoenzyme and thus increases transcriptional efficiency (Sakirau et al., PNAS, 1996, 93:9488-9492).

[0073] TFA2 Assays:

[0074] (a) ATLAS: CaTfa2 protein could be purified and challenged with an environmental condition, such as higher temperature or reduced pH, that unfolds the protein. A compound that binds to CaTfa2 protein may stabilize the native conformation of the protein.

[0075] (b) Two-hybrid interruption screen using another interacting protein: CaTfa2 and CaTfa1 could be placed into yeast two-hybrid screening vectors, one as the bait and one as the target. Binding by the two proteins will induce expression of a reporter gene. A compound that interferes in the binding of the two proteins should disrupt the induction of the reporter gene, allowing such compounds to be identified in a screening format. Interacting proteins other than CaTfa1p could be used in this format, notably CaGa111 protein.

NAB2

[0076] Nascent RNA polymerase II transcripts associate with nuclear ribonucleoproteins and remain associated during the subsequent RNA processing reactions, such as pre-mRNA polyadenylation and splicing and transport to the cytoplasm. Saccharomyces cerevisiae NAB2 is one of the major proteins associated with polyadenylated RNA in vivo and is essential for cell growth (Anderson, J. T., et al., Molecular and Cellular Biology, 1993; 13:2730-2741). The NAB2 gene product is localized primarily to the nucleus (Anderson, J. T., et al., Molecular and Cellular Biology, 1993; 13:2730-2741). Two different RNA-binding motifs are identifiable in the sequence of NAB2: an RGG box observed in a variety of heterogenous nuclear RNA-binding proteins, and CCCH motif repeats related to the zinc-binding motifs of the largest subunit of RNA polymerases (Anderson, J. T., et al., Molecular and Cellular Biology, 1993; 13:2730-2741). NAB2 gene product interacts with the product of yeast KAP104, a gene encoding a karyopherin shown to function in the nuclear import of proteins, and has been shown to interact with human transportini (hTRN1), the human homolog of yeast KAP104 (Aitchison, J. D., et al., Science, 1996; 274:624-627;Truant, R., et al., Molecular and Cellular Biology, 1998; 18:1449-1458; M. C. Siomi, et al., Molecular and Cellular Biology, 1998; 18:4141-4148).

[0077] NAB2 Assays:

[0078] (a) ATLAS: CaNab2 protein could be purified and challenged with an environmental condition, such as higher temperature or reduced pH, that unfolds the protein. A compound that binds to CaNab2 protein may stabilize the native conformation of the protein.

[0079] (b) Two-hybrid interruption screen using another interacting protein: CaNAB2 and CaKAP104 could be placed into yeast two-hybrid screening vectors, one as the bait and one as the target. Binding by the two proteins will induce expression of a reporter gene. A compound that interferes in the binding of the two proteins should disrupt the induction of the reporter gene, allowing such compounds to be identified in a screening format. Interacting proteins other than CaKap104p could be used in this format.

[0080] (c) RNA-binding screen: Compounds could be screened for their ability to interfere with the binding of RNA by CaNab2 protein. The binding of RNA and CaNab2 protein could be assessed in a variety of ways: 1) through capture on a filter or capture by antibodies; 2) in homogeneous solution using fluorescently-labeled RNA and detection of a change in fluorescence polarization; or 3) detection of a gel shift when RNA is bound by the protein.

MPT1

[0081] MPT1 is a target that has been identified in both S. cerevisiae and C. albicans. MPT 1 proteins have not been characterized in detail. ScMPT1 was isolated in a two-hybrid screen using ScPrp9 as bait (Froniont-Racine, M., et al., Nat Genet, 1997; 16:277-82). Prp9 is a subunit of a complex involved in RNA splicing. The fact that ScMPT1 would interact with Prp9 suggests that ScMPT1 would also be involved in RNA splicing. Validation data in S. cerevisiae and C. albicans indicate that MPT 1 is important for fungal cell growth and viability, which may correlate with its putative function in RNA splicing. A mammalian homolog has been proposed, but the degree of homology is too low to be confident about this. The apparent importance of MPT1 for fungal growth combined with the absence of a highly similar protein in mammalian cells make MPT1 an excellent target for antifungal drug discovery.

[0082] MPT1 assays:

[0083] (a) ATLAS. (See above).

[0084] (b) Cell-based assays: Various strains of S. cerevisiae could be constructed in which ScMPT1 would be replaced with a functional MPT1 gene (i.e., derived from cDNA when necessary) from different organisms, in particular fungi and mammals. These cells would be grown in individual wells containing defined number and mixtures of compounds, which potentially could inhibit growth. Differences in degrees of inhibition by compounds between above-mentioned strains may suggest that a compound may inhibit growth by preferentially inhibiting activity of a class of MPT1.

[0085] (c) Protein-protein interaction based assays: (i) Two-hybrid screen (Fromont-Racine, M., et al., Nat Genet, 1997; 16:277-82) using MPT1 and PRP9 (or any other protein found to interact with MPT1); (ii) Direct binding assay: The interacting protein could be fixed onto a carrier an allowed to bind easily detectable MPT1. In the absence of inhibitors, a high signal would result. However, interference with this interaction may reduce signal. The orientation of the assay could also be reversed by fixation of MPT1 and incubation with a interacting protein labeled with a reporter molecule such as, e.g., a radionucleotide or a fluorescent compound.

MTR2

[0086] In eukaryotic cells, mRNA transport is an important cellular process for gene expression and regulation. A set of genes were identified through an attempt to isolate Saccharomyces cerevisiae temperature-sensitive mutants that accumulate poly(A) RNA in the nucleus.(Kadowaki, T., et al., J Cell Biol, 1994; 126, 649-59) One of the genes, MTR2 encodes a 21 kD nuclear protein that shows a limited homology to a E. coli protein implicated in plasmid DNA transfer.(Kadowaki, T., et al., J Cell Biol, 1994; 126, 649-59) It has been shown that Mtr2 protein can interact with a nuclei pore associated protein, Mex67p and their interaction appears to be essential for mRNA export. (Santos-Rosa, H., et al., Mol Cell Biol, 1998; 18:6826-38) Genetic and biochemical evidence also indicated that Mtr2p can interact with Nup85p, suggesting that Nup85p might be the target at nuclei pore complex (NPC) to which Mtr2p and Mex67 bind.(Santos-Rosa, H., et al., Mol Cell Biol, 1998; 18:6826-38) Given all these factors, it was proposed that Mtr2 protein is the key component of mRNA export machinery in yeast. (Santos-Rosa, H., et al., Mol Cell Biol, 1998; 18:6826-38; Schneiter, R., et al., Mol Biol Cell, 1995; 6:357-70)

[0087] Recently, a human homolog of Mex67, TAP was identified that can interact with poly(A) RNA and human nucleoporin. However, no Mtr2 human homolog was found so far. Katahira et al (The Mex67p-mediated nuclear mRNA export pathway is conserved from yeast to human. Embo Journal 18, 2593-2609 (1999)) identified a small human protein, p15 that interact with TAP. Interestingly, co-expression of TAP and p15 in yeast can functionally complement Mex67-Mtr2 complex suggesting the existence of the evolutionarily conserved pathway that is involved in mRNA transport.

[0088] MTR2 assays:

[0089] (a) ATLAS: Mtr2 protein can be purified to homogeneity. Challenging purified Mtr2 protein with different environment conditions such as higher temperature or reduced pH will result in the protein conformation change leading protein to the unfolding state. Any compound that binds to Mtr2 will potentially stabilize protein in the native state. Using ATLAS can help identify compound that binds to Mtr2.

[0090] (b) Two hybrid with Mex67. Mtr2 and Mex67 can be used as a pair of genes in yeast with one of them as the bait and the other used as target. Binding of Mtr2 and Mex67 protein in yeast will result in the induction of a reporter gene that can be detected. Any compound that interrupts the interaction of Mtr2pand Mex67p will disrupt the induction of the reporter gene and thus that compound can be identified.

[0091] (c) Two hybrid with Nup85p. Mtr2 and Nup85 can be used as a pair of genes in yeast with one of them as the bait and the other used as target. Binding of Mtr2 and Mex67 protein in yeast will result in the induction of a reporter gene that can be detected. Any compound that interrupts the interaction of Mtr2p and Nup85p will disrupt the induction of the reporter gene and thus that compound can be identified.

BOS1

[0092]Saccharomyces cerevisiae BOS1 is an essential gene that functions in ER-to-Golgi transport. The protein is a cytoplasmically-oriented type II integral membrane protein of secretory vesicles (Newman et al., Embo J.,1992, 11:3609-3617; Lian et al., Cell, 1993, 73:735-745). Depletion of BOS1 results in a block in ER-to-Golgi protein transport and accumulation of small vesicles (Shim et al., J. Cell Biol., 1991, 13:55-64). The gene was originally isolated as a high copy suppressor of BET1 (Newman et al., Embo J., 1992, 11:3609-3617). BOS1 exhibits genetic and physical interactions with several proteins known to be involved in vesicular transport from the ER to the Golgi. In addition to suppressing BET1 defects, BOS1 overexpression can also overcome defects in SEC22 and YPT1 (Newman et al. Embo Journal 11, 3609-17(1992)). Bos1p has been shown to pair with Sec22p under the influence of Ypt1. Bos1p, Bet1p and Sec22p are V-SNARE proteins (Lian et al., Cell 73, 735-45 (1993); Pfeffer, Annu. Rev. Cell Dev. Biol. 12, 441-461 (1996)) that form a complex involved in transport vesicle docking (Ferro-Novick et al., Cell Biophys 19, 25-33 (1991)). YPT1 is a Rab protein required for SNARE complex formation (Sogaard et al., Cell 78, 937-48 (1994); Lian et al., Nature 372, 698-701 (1994); Lazar et al., Trends Biochem Sci 22, 468-472 (1997)). The V-SNAREs Bos1p and Sec22p cooperatively interact with the t-SNARE Sed5p prior to membrane fusion (Sacher et al., J Biol Chem 272, 17134-8 (1997)).

[0093] BOS1 assays:

[0094] (a) BOS1 is a good ATLAS assay target. In addition, defects in BOS1 function could be assessed in a reconstituted transport system (Lian, J. P., and Ferro-Novick, S. Bos1p, Cell, 1993; 73:735-45) or in a cell-based assay of invertase secretion (Johnson, L. M., et al.,Cell, 1987; 48:875-885) that monitors the inefficient transport of secreted protein from the ER to the Golgi (Shim, J., et al., J Cell Biol, 1991; 113:55-64).

[0095] (b) In vitro transport system (Lian et al., Cell 73, 735-45 (1993)).

[0096] (c) Cell-based assay of invertase secretion (Johnson et al., 1987) that monitors the inefficient transport of secreted protein from the ER to the Golgi (Shim et al., 1991).

[0097] (d) Protein:protein interactions. BOS1 has multiple protein partners (see above) whose interactions can be monitored by assayed by two-hybrid analysis or in vitro protein binding assays.

POL30

[0098] References for this section are numbered at the end of the section.

[0099]Saccharomyces cerevisiae POL30 is an essential gene and encodes the yeast proliferating cell nuclear antigen (PCNA) (Bauer et al., NAR, 1990, 18: 261-5). The structure of yeast PCNA has been determined, and it appears to function as a trimer that forms a sliding clamp around the DNA double helix (Krishna et al., J Mol Biol, 1994, 241: 265-8). PCNA can load onto the ends of linear DNA molecules in vitro, but efficient loading of PCNA onto DNA requires ATP and the product of RFC1 (McAlear et al., Genetics, 1996, 142:65-78, Burgers et al., J Biol. Chem., 1993, 268: 19923-19926).

[0100] PCNA is required for both DNA synthesis and DNA repair in mammals and yeast. PCNA interacts with DNA polymerase delta or epsilon to enhance processive replication of DNA (Holmes et al., Cell, 1999, 96: 415-424). PCNA interacts with FEN-1, the product of the mammalian homolog of RAD27, a protein required for Okazaki fragment processing (Ishimi et al., J. Biol.Chem., 1988,263: 19723-19733; Li et al., J. Biol. Chem., 1995, 270:22109-22112; Turchi et al., PNAS, 1995, 91:9803-9807). PCNA is required in vitro for reconstitution of nucleotide excision repair and base excision repair reactions. (Ayyagari et al., Mol Cell Biol, 1995, 15:4420-0; Umar et al., Cell, 1996, 87:65-73; Johnson et al, J Biol Chem, 1996, 271:27987-90; Matsumoto et al., Mol Cell Bio., 1994, 14:6187-97; Nichols et al., NAR, 1992 10:2441-2446; Shivji et al., Cell, 1992, 69:367-374). Transcription silencing may also involve PCNA (Ehrenhofer-Murray et al., Genetics, 1999, 153:1171-82).

[0101] POL30 assays:

[0102] (a) ATLAS: CaPo130 protein could be purified and challenged with an environmental condition, such as higher temperature or reduced pH, that unfolds the protein. A compound that binds to CaPo130 protein may stabilize the native conformation of the protein.

[0103] (b) Two-hybrid interruption screen using CaRad27 protein or another interacting protein: CaPo130 and CaRad27 could be placed into yeast two-hybrid screening vectors, one as the bait and one as the target. Binding by the two proteins will induce expression of a reporter gene. A compound that interferes in the binding of the two proteins should disrupt the induction of the reporter gene, allowing such compounds to be identified in a screening format. Interacting proteins other than CaRad27p could be used in this format. A screen could be designed to interfere with the multimerization of CaPo130 by using the gene as both bait and prey.

[0104] (c) DNA-binding screen: Compounds could be screened for their ability to interfere with the binding of DNA to CaPo130 protein. The binding of DNA and CaPo130 protein could be assessed in a variety of ways: 1) through capture on a filter or capture by antibodies; 2) in homogeneous solution using fluorescently-labeled DNA and detection of a change in fluorescence polarization; or 3) detection of a gel shift when DNA is bound by the protein.

YMR131C

[0105] YMR131C is an essential gene in C. albicans. Nearest human match is a 25% identity to human retinoblastoma protein RBBP4. YMR131 C protein has WD40 repeats suggesting that it may physically interact with other proteins. Recent report suggests that the protein may be involved in the nucleopore complex formation (Rout, M., et al., J. Cell Biol., 2000; 148:635-652).

[0106] YMR131C assays:

[0107] (a) ATLAS

[0108] (b) If a mammalian YMR131C Homolog is found that complements C albicans YMR131C, a cell-based assay could be set up to measure cell growth in the presence/absence of a compounds comparing strains with C. albicans YMR131C and human YMR131C Homolog.

[0109] (c) If proteins that physically interact with YMR131C are identified, two-hybrid system based assay can be developed to monitor interaction between YMR131C and another protein.

[0110] (d) If YMR131C is essential for nuclear pore transport, an assay can be set up to monitor efficiency of transport through nuclear pores.

SQT1

[0111]Saccharomyces cerevisiae SQT1 is an essential gene, which encodes a 60S ribosomal subunit protein required for joining of 40S and 60S subunits (Eisinger et al., MCB, 17:5146-5155, 1997). SQT1 was isolated as a suppressor of dominant-negative truncation mutations of ribosomal protein QSR1 (Eisinger et al., MCB, 17:5136-5145, 1997; Eisinger et al., MCB, 17:5146-5155, 1997). The loss of SQT1 function results in the formation of half-mer polysomes whereby the 40S and 60S subunits fail to join. SQT1 may be required for the assembly of QSR1 onto the 60S ribosomal subunit (Eisinger et al., MCB, 17:5146-5155, 1997). The protein may be part of an oligomeric complex and is localized to the cytoplasm where it is loosely associated with ribosomes (Eisinger et al., MCB, 17:5146-5155, 1997).

[0112] SQT1 assays:

[0113] (a) SQT1 is a good candidate for an ATLAS assay. In addition, polysome and ribosome subunit analysis could be carried out in a low-throughput secondary assay. Interference with SQT1 function should result in half-mer polysome profiles. This type of assay would involve isolation and fractionation of ribosomal subunits, 80S ribosomes and polysomes on sucrose velocity gradients (Eisinger et al., MCB, 17:5136-5145, 1997).

[0114] (b) Polysome and ribosome subunit analysis could be carried out in a low-throughput secondary assay. Interference with SQT1 function should result in half-mer polysome profiles. This type of assay would involve isolation and fractionation of ribosomal subunits, 80S ribosomes and polysomes on sucrose velocity gradients (Eisinger et al., 1997a).

MTW1

[0115] MTW1 is an essential protein in C. albicans with unknown function. Mtw1p (Mis twelve-like protein) is 33% identical to S. cerevisiae Mis12p. The published data suggests that S. pombe Mis12p is required for centromere structure maintenance and correct spindle morphogenesis during chromosomal segregation (Goshima et al., Gen. Dev., 13:1664-1677, 1999). It is possible that C. albicans Mtw1p has DNA-binding motifs. No true human homolog has been identified so far.

[0116] MTW5 assays:

[0117] (a) ATLAS

[0118] (b)If MTW1 binds to DNA, an assay for DNA-binding activity can be set up.

[0119] (c) If a mammalian MTW1 homolog is found which complements C albicans MTW1, a cell-based assay can be set up to measure cell growth in the presence/absence of a compound, comparing strains with C. albicans MTW1 and the human MTW1 homolog.

[0120] (d) If proteins that physically interact with MTW1 are identified, two-hybrid system based assays can be developed to monitor interaction between MTW1 and other proteins.

TFB1

[0121] RNA polymerase II needs five additional general transcription factors for promotor dependent transcription, one of which is TFIIH (Svejstrup et al., J Biol Chem, 269:28044-8, 1994). TFIIH contains DNA-dependent ATPase activity and protein kinase activity directed against the C-terminal Repeat Domain of RNA polymerase II. TFB1 is one of the subunits of TFIIH and is needed for both transcription and nucleotide excision repair.

[0122] TFB1 genes have been found in both mammalian and fungal cells. However, the degree of conservation between fungi is higher than that between fungi and mammalian (approximately 40% vs. 20%). This difference combined with the importance for fungal cell viability makes TFB1 an excellent target for antifungal drug discovery.

[0123] TFB1 assays:

[0124] (a) ATLAS

[0125] (b) RNA polymerase II promotor-dependent transcription assay

[0126] (c) Cell-based assay: Various strains of S. cerevisiae would be constructed in which ScNIP1 would be replaced with a functional TFB1 gene (i.e. derived from cDNA when necessary) from different organisms, in particular fungi and mammals. These cells would be grown in individual wells containing defined number and mixtures of compounds, which potentially could inhibit growth. Differences in degrees of inhibition by compounds between above-mentioned strains suggest that a compound may inhibit growth by preferentially inhibiting activity of a class of TFB1.

[0127] (d) Protein-protein/DNA interaction based assay: (i) Two-hybrid screen (Fromont-Racine et al., Nat Genet, 16:277-82, 1997) using TFB1 and any protein (or DNA) found to interact with TFB1 (e.g. other TFIIH subunits); (ii) Direct binding assay: The interacting protein or DNA would be fixed onto a carrier an allowed to bind easily detectable TFB1. In the absence of inhibitors a high signal would result. However, interference with this interaction would reduce signal. Orientation of the assay could also be reversed by fixation of TFB1 and incubation with labeled interacting protein/DNA.

SPC98

[0128]Saccharomyces cerevisiae SPC98 encodes an essential protein that has a role at the spindle pole body (SPB), the fungal equivalent of the centrosome. SPC98 was identified as a high copy suppressor of a mutation in TUB4, the yeast gene for gamma-tubulin. A conditional mutation in SPC98, when shifted to restrictive conditions, results in a cell-cycle arrest with defective mitotic spindles (Geissler, et al., Embo Journal, 15:3899-911, 1996). SPC97, a gene that has regions of sequence similarity to SPC98, was identified as a high copy suppressor of a mutation in SPC98 (Knop et al., Embo Journal, 16:1550-64, 1997). The products of both SPC97 and SPC98 have been shown to form a complex with gamma tubulin and to be responsible for microtubule nucleation (Knop, M., et al, 1997; Pereira et al., Embo Journal, 18:4180-4195, 1999; Chen et al., J Cell Biol, 141:1169-1179, 1998). The human homologs of SPC97 and SPC98 are also in a complex with ganuma-tubulin and appear to have the same functions (Tassin et al., J Cell Biol, 141:689-701, 1998; Murphy et al., J Cell Biol, 141:663-74, 1998).

[0129] SPC98 Assays:

[0130] (a) ATLAS: CaSpc98 protein could be purified and challenged with an environmental condition, such as higher temperature or reduced pH, that unfolds the protein. A compound that binds to CaSpc98 protein may stabilize the native conformation of the protein.

[0131] (b) Two hybrid interruption screen using another interacting protein: CaSpc98 and CaSpc97 could be placed into yeast two-hybrid screening vectors, one as the bait and one as the target. Binding by the two proteins will induce expression of a reporter gene. A compound that interferes in the binding of the two proteins should disrupt the induction of the reporter gene, allowing such compounds to be identified in a screening format. Interacting proteins other than CaSpc97 could be used in this format.

BFR2

[0132]Saccharomyces cerevisiae BFR2 is an essential gene that was isolated as a high copy suppressor of the growth defects induced by Brefeldin A (BFA), a fungal metabolite that disrupts Golgi structure and function (Chabane et al., Curr. Genet, 33:21-8, 1998; Takatsuki et al., Agric. Biol. Chem., 49:899-902, 1995; Klausner et al., J. Cell Biol., 116:1071-1080, 1992). In addition, BFR2 overproduction was shown to partially suppress the growth defects of four mutants involved in the secretory pathway (Chabane et al. 1998). The mutants, sec13-1, sec16-1, sec23-1 and ypt1-1, are each involved in budding and or docking of small vesicles en route to the Golgi. Thus, it was suggested that BFR2 is involved in protein transport (Chabane et al. 1998).

[0133] BRF2 assays:

[0134] (a) BFR2 can be screened in an ATLAS assay format; and

[0135] (b) Based on the proposed function of BFR2, compound interference with BFR2 would make cells more highly sensitive to BFA. Therefore, increased cellular sensitivity to BFA is an additional assay that could be used as a secondary screen.

RNA1

[0136]Saccharomyces cerevisiae RNA1 gene encodes the Rna1 protein, which is involved in nuclear export of all types of RNA (Sarkar et al. Mol Biol Cell, 1998, 9:3041-55). It is required for export of assembled 60S ribosomal subunits from the nucleus to the cytoplasm (Hurt et al., J Cell Biol, 1999, 144:389-401). Rna1p plays a direct role in the import of proteins into the nucleus (Corbett et al., J Cell Biol, 1995, 130:1017-26). GST-Rna1p catalytically stimulates GTP hydrolysis by purified Gsp1p (Corbett et al., J Cell Biol, 1995, 130:1017-26). It does not stimulate GTPase activity of ras or Rab7 (Becket et al., J Biol Chem, 1995, 270:11860-5). RNA1 has extensive homology to S. pombe Rna1p and to the mammalian Ran/TC4 GTPase activating protein (Corbett et al., J Cell Biol, 1995, 130:1017-26; Bischoff et al., PNCAS USA, 1995 92:1749-53; Melchior et al., Mol Biol Cell, 1993 4:569-81). The rna1-1 mutant is complemented by S. pombe rna1. It is a member of superfamily of proteins that have leucine-rich repeat motifs, which can be up to 29 amino acids in length (Melchior et al., Mol Biol Cell, 1993 4:569-81; Schneider et al., Mol Gen Genet, 1992, 233: 315-8). Cytosolic extracts made from rna1-1 mutants are completely devoid of Rna1p and the protein was found to be localized within the nucleus (Traglie et al., PNCAS USA, 1996, 93:7667-72). The mutant affects RNA processing and export from nucleus although Rna1p is cytoplasmic (Hopper et al., J Cell Biol, 1990, 111:309-21). rna1-1 mutant accumulates intron-less and intron-containing tRNA in the nucleus at the nonpermissive temperature (Sarkar et al. Mol Biol Cell, 1998, 9:3041-55). It shows altered export of RNA from nucleus to cytoplasm with RNA accumulating at the nuclear periphery (Amberg et al., GAD, 1992 6:1173-89). The temperature-sensitive mutant has accumulation of 35S pre-rRNA (Venema et al., Yeast, 1995, 11:1629-50). The rna1-1 mutant abolishes nuclear pore complex localization of Cse1p-GFP, which becomes distributed throughout the cell (Hood et al., J Biol Chem, 1998, 273:35142-35146). When the 11 amino acids from the carboxy terminal are removed, the protein retains its function (Traglia et al., Mol Cell Biol, 1989, 9:2989-99). In rna1-1 mutant, export of the small ribosomal subunit from the nucleus is directly inhibited with accompanying secondary defects in processing of pre-rRNA (Moy et al., GAD, 1999, 13:2118-2133).

[0137] RNA1 assays:

[0138] (a) ATLAS

[0139] (b) Mutants of RNA1 accumulates intron-less and intron-containing tRNA (1). This information may be useful in assaying such tRNA in presence/absence of compounds that bind and disrupt Rna1p activity.

[0140] (c) The defects in processing of ³⁵S pre-rRNA may be monitored by probing with oligonucleotides near the pre-rRNA cleavage sites by Northern Hybridization and primer extension analysis.

[0141] (d) There is accumulation of ³⁵S pre-rRNA in temperature sensitive mutants (11). This effect may be studied in a cell-based assay. Levels of ³⁵S-labeled pre-rRNA may be assayed in presence/absence of a compound.

GCD7

[0142] Eukaryotic protein translation is initiated by acquisition of mRNA and Met-tRNAiMet by the 40S ribosomal subunit. These changes are mediated by Initiation Factors (eIF's). eIF2 forms a complex with Met-tRNAiMet and GTP, which binds to 40S ribosomes (Pavitt et al., Mol Cell Biol, 1997, 17:1298-313). After subsequent binding of mRNA to these 40S ribosomes and recognition of the AUG codon by Met-tRNAiMet, GTP hydrolysis releases eIF2-GDP. eIF2-GDP is converted to eIF2-GTP by eIF2B, a guanine nucleotide exchange factor, as a result of which protein translation can continue. Starvation for amino acids leads to phosphorylation of eIF2, reduction of recycling of eIF2-GDP by eIF2B and preferential translation of GCN4, a transcriptional activator of amino acid biosynthetic enzymes. eIF2B is composed of 5 subunits of which 4, including GCD7, are essential for growth. GCD7 seems to form part of the binding site for phosphorylated-eIF2 thereby mediating inhibition of eIF2B.

[0143] GCD7 genes have been found in both mammalian and fungal cells. However, the degree of conservation between fungi is higher than that between fungi and mammalian (approximately 50% vs. 35%). This difference combined with the importance for fungal cell viability makes GCD7 an excellent target for antifungal drug discovery.

[0144] GCD7 assays:

[0145] (a) ATLAS

[0146] (b) Protein translation assay (Colthurst, et al., J Gem Microbiol, 1991, 137:851 -857)

[0147] (c) Cell-based assays: (i) Various strains of S. cerevisiae could be constructed in which ScGCD7 would be replaced with a functional GCD7 gene (i.e., derived from cDNA when necessary) from different organisms, in particular fungi and mammals. These cells would be grown in individual wells containing defined number and mixtures of compounds, which potentially could inhibit growth. Differences in degrees of inhibition by compounds between above-mentioned strains suggest that a compound may inhibit growth by preferentially inhibiting activity of a class of GCD7; (ii) Instead of measuring growth dependent on the presence of inhibitory compounds a more specific assay aimed at expression of GCN4 could be performed. Histidine starvation would be induced with AT thereby making expression of GCN4 required for growth. Alternatively, cells could be grown to higher densities prior to addition of AT and GCN4 activation could be monitored by transcriptional (or translational) fusions of the GCN promotor (plus (part of) Gcn4p) to a suitable reporter gene/protein (Pavitt et al., Mol Cell Biol, 1997, 17:1298-313).

[0148] (d) GDP exchange assays (Cigan et al., PNAS, 1993, 90:5350-5354): eIF2 and eIF2B would be isolated from an appropriate host. eIF2 would complexed with labeled GDP. Incubation of this complex will release labeled GDP, which would be separated from the complex. Compound interference with this liberation would leave high amounts of label.

[0149] (e) Protein-protein interaction based assays: (i) A two-hybrid screen (Fromont-Racine et al., Nat Genet, 1997, 16:277-82) using GCD7 and any protein found to interact with GCD7 (e.g. other eIF2 subunits); (ii) A direct binding assay. The interacting protein would be fixed onto a carrier an allowed to bind easily detectable GCD7. In the absence of inhibitors, a high signal would result. However, interference with this interaction would reduce the signal. Orientation of the assay could also be reversed by fixation of GCD7 and incubation with labeled interacting protein.

SKI6

[0150] Most strains of Saccharomyces cerevisiae carry one or more dsRNA viruses. Yeast harboring these viruses are called killer strains and secret toxin which is lethal to most of the ones that carry no viruses. Derepression of toxin expression results in superkiller phenotype (Ridley et al., Mol Cell Biol, 1984, 4:761-70).

[0151] SKI6 is one of the many genes that were identified by the superkiller phenotype of mutants. (Masison et al., Mol Cell Biol, 1995, 15:2763-71) It encodes an essential protein that is homologous to bacterial tRNA-processing enzyme, RNase PH. (Lussier et al., Genetics, 1997, 147:435-450;Mitchell et al., Cell, 1997, 91:457-466) Benard et. al. discovered that ski6 mutation bypassed the requirement of polyA tail for efficient mRNA translation, allowing better translation of non-polyA mRNA, including L-A virus mRNA. (Benard et al., Mol Cell Biol, 1998, 18:2688-2696) Later experiments suggested that SKI6 plays an important role in 3′-5′ mRNA decay which is consistent with the fact the ski6 mutant derepresses the virus mRNA translation. (Mitchell et al., Cell, 1997, 91:457-466;vanHoof et al., Cell, 1999, 99:347-350)

[0152] SKI6 also functions in ribosomal RNA processing. (Allmang et al., GAD, 1999, 13:2148-58) It is a part of exosome complex that functions as 3′-5′ exoribonuclease that is required for 5.8S rRNA maturation. (Mitchell et al., Cell, 1997, 91:457-466)

[0153] SKI6 Ski6p can be screened by 3 ′-5′ exoribonuclease activities. RNA substrate will be radiolabeled with P-32 and incubated with recombinant purified Ski6p. Loss of TCA precipitable radiolabeled RNA substrate is due to the activity of Ski6 protein, and inhibitors of Ski6p can thereby be screened.

[0154] (a) ATLAS: Ski6 protein can be purified to homogeneity. Challenging purified Ski6 protein with different environment conditions such as higher temperature or reduced pH will result in the protein conformation change leading to the unfolding state. Any compound that binds to Ski6 can potentially stabilize protein in the native state. Using ATLAS can help identify compound that binds to Ski6p.

[0155] (b) Luciferase assay. Luciferase messenger RNA with or without PolyA tails can be prepared and transfected into yeast through electroporation. Since Ski6p blocks translation of non-polyA mRNA, Luciferase activity will be high with mRNA that contains polyA tails and about 40 times lower with mRNA that has no polyA tails. In the presence of compound that block the activity of Ski6p, luciferase activity in the presence of mRNA that contains polyA tails should remain relatively the same while activity in the absence of polyA tail should increase about 10 times.

NIP1

[0156] Eukaryotic protein translation is a initiated by acquisition of mRNA and Met-tRNAiMet by the 40S ribosomal subunit (Hanachi et al., J Biol Chem, 1999, 274:8546-8553). These changes are mediated by Initiation Factors (eIF's). eIF3 is composed of approximately 8-10 subunits, one of which is NIP1. No specific, enzymatic function of NIP1 within eIF3 has been described. However, validation of this gene in C. albicans and S. cerevisiae indicates that the protein is important for cell growth and viability.

[0157] NIP1 genes have been found in both mammalian and fungal cells. However, the degree of conservation between fungi is higher than that between fungi and mammalian (approx. 40% vs. 25%). This difference combined with the importance for fungal cell viability makes NIP1 an excellent target for antifungal drug discovery.

[0158] NIP1 assays:

[0159] (a) ATLAS

[0160] (b) Protein translation assay (Colthurst et al., J Gen Biol, 1991, 137:851-857)

[0161] (c) Cell-based assays: Various strains of S. cerevisiae would be constructed in which ScNIP1 would be replaced with a functional NIP1 gene (i.e. derived from cDNA when necessary) from different organisms, in particular fungi and mammals. These cells would be grown in individual wells containing defined number and mixtures of compounds, which potentially could inhibit growth. Differences in degrees of inhibition by compounds between above-mentioned strains suggest that a compound may inhibit growth by preferentially inhibiting activity of a class of NIP1.

[0162] (d) Protein-protein interaction based assays: (i) A two-hybrid screen (Fromont-Racine et al., Nat Genet, 1997, 16:277-82) using NIP1 and any protein found to interact with NIP1 (e.g. other eIF3 subunits); (ii) Direct binding assay: The interacting protein would be fixed onto a carrier an allowed to bind easily detectable NIP1. In the absence of inhibitors a high signal would result. However, interference with this interaction would reduce signal. Orientation of the assay could also be reversed by fixation of NIP1 and incubation with labeled interacting protein

LCP5

[0163] LCP5 is an essential Saccharomyces cerevisiae gene which encodes a 40.8 Kd protein. LCP5p immunolocalizes to the nucleolus and participates in the early cleavage events at sites A0 to A2 in the pathway of pre-rRNA processing (Wiederkehr et al., RNA, 1998, 4:1357-1372). Depletion leads to reduced levels of 18S ribosomal subunits with concomitant accumulation of 60S ribosomal subunits and a sharp reduction in polysomes (Wiederkehr et al., RNA, 1998, 4:1357-1372). An lcp5-1 mutant shows increased sensitivity to the aminoglycoside antibiotics paromomycin and neomycin, and to cycloheximide, indicating a defect in translation (Wiederkehr et al., RNA, 1998, 4: 1357-1372). lcp5-1 mutant, or depletion of Lcp5p, shows sharp reduction of 18S rRNA, with accumulation of an aberrant 23S pre-rRNA species (Wiederkehr et al., RNA, 1998, 4:1357-1372).

[0164] LPC5 assays:

[0165] (a) ATLAS

[0166] (b) Lcp5 mutant shows predominant processing at site A3 and reduced cleavage at sites A0 and A2 in the 35S pre-rRNA (Wiederkehr et al., RNA, 1998, 4:1357-1372). The defects in processing of ³⁵S pre-rRNA may be monitored by probing with oligonucleotides near the pre-rRNA cleavage sites by Northern Hybridization and primer extension analysis.

[0167] (c) The rRNA metabolism may be affected by LCP5 specific compounds and this may be monitored by looking at the total RNA which will show a decrease in the steady state amounts of 18S rRNA (Wiederkehr et al., RNA, 1998, 4:1357-1372).

[0168] (d) Compounds may be assayed in presence/absence of alminoglycoside antibiotics paromomycin and neomycin, and to cycloheximide. Since mutant shows an increased sensitivity to these antibiotics (Wiederkehr et al., RNA, 1998, 4:1357-1372), a synergystic effect may be observed.

NCE103

[0169] In a search for components of protein export machinery, Cleves et al (Cleves et al., J Cell Biol., 1996, 133(5):1017-26) discovered NCE103 gene that is involved in non-classic export pathway that functions independent of the classical pathway through ER and the Golgi compartments. (Cleves et al., J Cell Biol., 1996, 133(5):1017-26) Even though NCE103 gene appeared to be essential under normal conditions, experiments by Gotz et al suggested that it grew like wild-type under anaerobics conditions. (Gotz, et al., Yeast, 1999, 15:855-864) The predicted amino acid sequence of Nce103p shows high levels of identities to carbonic anhydrase of both prokaryotes and eukaryotes. (Gotz, et al., Yeast, 1999, 15:855-864) Expression of Medicago sativa carbonic anhydrase gene in a high-copy number plasmid complement the growth defects caused by nce103 deletion. (Gotz, et al., Yeast, 1999, 15:855-864) Given that nce103 deletion strain grow like wild-type under anaerobic conditions and null deletion can be complemented by Medicago sativa carbonic anhydrase gene, it was proposed that nce103 functions as an authentic carbonic anhyrase and is required for protection against certain products of oxidative metabolites under aerobics condition. (Gotz, et al., Yeast, 1999, 15:855-864)

[0170] NCE103 assays:

[0171] (a) ATLAS: Nce103 protein can be purified to homogeneity. Challenging purified Nce103 protein with different environment conditions such as higher temperature or reduced pH will result in the protein conformation change leading protein to the unfolding state. Any compound that binds to Nce103p can potentially stabilize protein in the native state. Using ATLAS can help identify compound that binds to Nce103p.

ECO1

[0172]Saccharomyces cerevisiae ECO1 (also called CTF7) is an essential gene that is required to establish cohesion between sister chromatids during DNA replication. It was isolated as a mutant that can separate sister centromeres in the presence of Pds1p, an anaphase inhibitory protein (Toth et al., Genes and Dev., 13:320-333, 1999; Skibbens et al., Genes and Dev., 13:307-319, 1999). The protein is essential during S phase to establish sister chromatid cohesion but not during mitosis to maintain it (Skibbens et al., 1999). Cells harboring temperature-sensitive alleles of ECO1 arrest at restrictive temperature predominately as large budded cells with elongated spindles. There is a defect in separation of DNA such that mother cells often contain all the DNA (Skibbens et al., 1999). Some temperature-sensitive mutants display increased chormosome fragment loss at permissive temperature (Toth et al., 1999; Skibbens et al., 1999). The POL30 (DNA replication processivity factor or PCNA) gene in high copy can suppress ctf7 temperature sensitivity and chromosome loss thus lending further support of the hypothesis that CTF1/ECO1 functions in the establishment of sister chromatid cohesion (Skibbens et al., 1999).

[0173] ECO1 assays:

[0174] (a) ECO1 can be screened in an ATLAS format. Chromosome fragment loss can be assessed in a secondary assay. In this assay, faithful maintenance of a reporter chromosome fragment yields white colonies whereas loss of the reporter chromosome yields red sectored colonies (Toth et al., 1999; Skibbens, et al., 1999). In addition, the DNA content of cells can be analyzed by flow cytometry and in micrographs of cells stained with the nuclear dye, DAPI. (Toth et al., 1999).

[0175] (b) Chromosome fragment loss. Faithful maintenance of a reporter chromosome fragment yields white colonies whereas loss of the reporter chromosome yields red sectored colonies (Toth et al., 1999; Skibbens, et al., 1999).

[0176] (c) DNA content of cells can be analyzed by flow cytometry and in micrographs of cells stained with the nuclear dye, DAPI. (Toth et al., 1999).

ORC2

[0177]Saccharomyces cerevisiae ORC2 is a component of the 6-subunit origin recognition complex (ORC) that acts at the origins of DNA replication distributed throughout the length of chromosomes (Bell et al., Nature, 1992, 357:128-134). ORC2 is required for viability, and temperature sensitive mutations in ORC2 result in cell cycle arrest consistent with defects in DNA replication (Micklem et al., Nature, 1993, 366:87-89; M. Foss et al., Science, 1993, 262:1838-1844; Bell et al., Science, 1993, 262:1844-1849). ORC has been demonstrated to bind origins of replication by DNAse footprinting, and this activity is dependent on ORC2 (Bell et al., Science, 1993, 262:1844-1849; Lee et al., Mol Cell Bio, 1993, 262:1844-1849).The gene has also been shown to be required for transcriptional silencing and telomere silencing (Micklem et al., Nature, 1993, 366:87-89; M. Foss et al., Science, 1993, 262:1838-1844; Bell et al., Science, 1993, 262:1844-1849). These appear to be separable functions for the ORC2 gene product, since the role of ORC2 in silencing can be complemented in yeast by expression of Drosophila ORC2, but its role in replication is not complemented (Ehrenhofer-Murray et al., Science, 1995, 270:1671-1674).

[0178] ORC2 assays:

[0179] (a) ATLAS: CaOrc2 protein could be purified and challenged with an environmental condition, such as higher temperature or reduced pH, that unfolds the protein. A compound that binds to CaOrc2 protein may stabilize the native conformation of the protein.

[0180] (b) Two hybrid interruption screen using another interacting protein: CaOrc2 and a Candida albicans ortholog of another member of the ORC could be placed into yeast two-hybrid screening vectors, one as the bait and one as the target. Binding by the two proteins will induce expression of a reporter gene. A compound that interferes in the binding of the two proteins should disrupt the induction of the reporter gene, allowing such compounds to be identified in a screening format. Interacting proteins other than those in the ORC could be used in this format.

[0181] (c) DNA-binding screen: Compounds could be screened for their ability to interfere with the binding of DNA to CaOrc2 protein. The binding of DNA and CaOrc2 protein could be assessed in a variety of ways: 1) through capture on a filter or capture by antibodies; 2) in homogeneous solution using fluorescently-labeled DNA and detection of a change in fluorescence polarization; or 3) detection of a gel shift when DNA is bound by the protein. These screens may be done with other proteins in the ORC present during the assay.

CNS1

[0182] Hsp90 chaperone complexes maintain or restore activity in both heat-denatured proteins and signaling proteins prone to deactivation (Dolinski et al., Mol Cell Biol, 1998, 18:7344-7352). In present day models of Hsp90 complex interaction with signaling proteins (e.g., hormone receptors), a cycle is assumed to occur of contruction and degradation of an Hsp90-signaling protein complex into its subunits. When construction of the protein complex is complete, signaling can occur. However, if Hsp90 removal does not occur the signaling protein is degraded.

[0183] CNS1 is one of the Hsp90 chaperone complex subunits and is presumably bound via a Tetratrico Peptide Repeat (TPR) domain. CNS1 genes have been found in both mammnalian and fungal cells. However, the degree of conservation between fungi is higher than that between fungi and mammalian (approx. 55% vs. 30%). This difference combined with the importance for fungal cell viability makes CNS1 an excellent target for antifungal drug discovery

[0184] CNS1 assays:

[0185] (a) ATLAS

[0186] (b) Cell-based assays: Various strains of S. cerevisiae could be constructed in which ScCNS1 would be replaced with a functional CNS1 gene (i.e. derived from cDNA when necessary) from different organisms, in particular fungi and mammals. These cells would be grown in individual wells containing defined number and mixtures of compounds, which potentially could inhibit growth. Differences in degrees of inhibition by compounds between above-mentioned strains suggest that a compound may inhibit growth by preferentially inhibiting activity of a class of CNS1.

[0187] (c) Protein-protein interaction based assays: (i) Two-hybrid screen (Fromont-Racine et al., Nat Genet, 1997, 16:277-82) using CNS1 and any protein found to interact with CNS1 (e.g. other Hsp90 complex subunits); (ii) Direct binding assay: The interacting protein would be fixed onto a carrier an allowed to bind easily detectable CNS1. In the absence of inhibitors a high signal would result. However, interference with this interaction would reduce signal. Orientation of the assay could also be reversed by fixation of CNS1 and incubation with labeled interacting protein.

YPD1

[0188]Saccharomyces cerevisiae YPD1 is an essential gene that functions in a two-component regulatory system in the high-osmolarity sensing MAP kinase pathway. The protein mediates a transfer of a phosphate from Sln1p to Ssk1p under normal osmolarity to inhibit the MAP kinase kinase kinases Ssk2p and Ssk22p (Posas et al., Cell, 86:865-875, 1996). Ypd1 lethality is due to constant activation of the HOG1 pathway (Posas et al., 1996). The structure of Ypd1p has been solved and consists of a four-helix bundle that makes up the central core and contains the active site residue, His64. Residues around the active site are exposed to solvent and are important for phosphotransfer activity (Xu et al., J. Mol. Biol., 292:1039-1050, 1999).

[0189] YPD1 assays:

[0190] (a) YPD1 is a good candidate for an ATLAS screen. In addition, as a secondary in vitro assay, transfer of radiolabeled phosphate from Sln1p to Ypd1 can be monitored (Li et al., 1998).

[0191] (b) Transfer of radiolabeled phosphate from Sln1p to Ypd1 can be monitored in vitro (Li et al., EMBO J., 17:6952-6962, 1998).

TIM10

[0192] Tim10 was originally isolated as a suppressor of mrs2 mutant that is defect in mitochondria RNA splicing and respiration. (Jarosch et al., Mol Gen Genet, 1997, 255:157-65) Tim10 belongs to a group of evolutionary conserved protein called TIM family and shares extensive homology with another Tim protein, Tim9. (Bauer, et al., GEBS Lett, 1999, 464:41-47) Located in the mitochondria intermembrane space, it functions to transfer metabolic carrier proteins from cytoplasm to mitochondria. Tim10 is a soluble protein that forms a complex with Tim9 and Tim12 to bind to the precursor protein that is destined to the mitochondria and transfer them to another Tim complex, Tim 54-22-18. (Koehler et al., Science, 279:369-373, 1998; Sirrenberg et al., Nature, 391:912-915, 1998; Adam et al., Embo Journal, 18:313-319, 1999; Koehler et al., Embo J., 17:6477-6486, 1998; Endres et al., Embo J., 18:3214-3221, 1999). Tim 10 is essential for the biogenesis of mitochondria, as well as for viability of yeast cells. (Jarosch et al., Mol Gen Genet, 1997, 255:157-65) As a result of Tim10 depletion, mitochondria undergo dramatic changes in morphology and are unable to assemble cytochrome complexes. (Kubrich et al., J Biol Chem, 1998, 273:16374-16381)

[0193] TIM10 assays:

[0194] (a) ATLAS: Tim10 protein can be purified to homogeneity. Challenging purified Tim10 protein with different environment conditions such as higher temperature or reduced pH will result in the protein conformation change leading to the unfolding state. Any compound that binds to Tim10p can potentially stabilize protein in the native state. Using ATLAS can help identify compound that binds to Tim10p.

[0195] (b) Two-hybrid with Tim9. Even though, Tim10 has been shown to form a complex with Tim9 and Tim 12, only Tim10p direct interaction with Tim9p has been fully addressed. Screening compound that block Tim10 interaction with Tim9 using Two-hybrid will help identify compound that hit Tim10 protein. Tim10 and Tim9 can be used as a pair of genes in yeast with one of them as the bait and the other used as target. Binding of Tim10 and Tim9 protein in yeast will result in the induction of a reporter gene that can be detected. Any compound that interrupt binding of Tim10 protein and Tim9 protein will disrupt the induction of the reporter gene and thus that compound can be identified.

SRB4

[0196] SRB4 is an essential component of RNA polymerase II multisubunit complex (Thompson et al., Cell, 1993, 73:1361-75). SRB is known in the art to stand for Suppressor of RNA Polymerase B. SRB4 is required for RNA polymerase II transcription at most of the promoters (Thompson et al., PNAS, 1995, 92:4587-90). It has been recently demonstrated that SRB4 is dispensable for transcriptional activation of some genes depending on activation mechanism of a particular activator (Lee et al., Gen. Dev., 1999, 13:2934-9). DNA-crosslinking immunoprecipitation assay was used to show that activator-dependent stimulation of TBP binding requires Srb4 (Li et al., Nature, 1999, 399:605-9). C. albicans Srb4 protein has an intron and it is about 30% identical to its S. cerevisiae Homolog. SRB4 has a potential human homolog which is 20% identical.

[0197] SRB4 assays:

[0198] (a) ATLAS

[0199] (b) Cell-based assays can be set up to monitor transcriptional activation of a reporter gene in wild type strain and SRB4 temperature-sensitive strain.

[0200] (c) A two-hybrid system based assay can be developed to monitor interaction between Srb4p and other SRB proteins or RNA polymerase II CTD.

[0201] (d) In vitro transcription assay (Thompson et al., Cell, 1993, 73:1361-75, Koleske et al., Nature, 1994, 368:466-469).

Sequence Identities

[0202] The degree of sequence identity between the above S. cerevisiae (sc) genes and their C. albicans (ca) and, if available, human (hs) homologs are provided in Table 2. (See below). Multiple alignments were created using Clustal W (See Thompson et al., supra), and percentage identities caclulated using the GCG GAP program with a gap creation penalty of 12 and a gap extension penalty of 4. The sequence alignment results are also presented in the figures referred to in Table 2. TABLE 2 Sequence Identities S. cerevisiae Nominated targets gene genbank genbank C. albicans Human Sequence identities (%) half-life name orf name DNA protein source genbank # ca v sc sc y hs ca y hs FIG. 0.11 RPC34 YNR003C Z71618 CAA96279.1 stan-4-1929 U93869 50.4 28.3 27.3 1 0.34 POP3 YNL282W Z71558 CAA96194.1 gtc5417 n/a 26.1 — — 2 0.35 TFA2 YKR062W Z28287 CAA82141.1 stan-4-2738/gtc NP_002086 40.8 23.2 19.4 3 0.36 NAB2 YGL122C Z72644 CAA96830.1 stan-4-2144 AAD42873 32.2 22.5 22.8 4 0.37 MPT1 YMR005W Z48613 CAA88520.1 stan-4-2743/gtc CAA72189 36.7 23.3 19.2 5 0.39 MTR2 YKL186C Z28186 CAA82029.1 stan-4-3102 n/a 28.7 — — 6 0.44 BOS1 YLR078C X57792 CAA97636.1 stan-4-2841/gtc NP_003560 37.9 16.8 18.1 7 0.49 POL30 YBR088C Z35957 CAA85038.1 gtc2521 P12004 54.5 35.7 41.3 8 0.54 RSA2 YMR131C NC_001145 CAA88556.1 stan-4-2117 NP_005601 63 24 26.1 9 0.68 SQT1 YIR012W U75717 AAB69630.1 stan-4-3094 NP_001078 44.5 22.9 25.1 10 0.81 MTW1 YAL034W-A AB027473 BAA77792.1 stan-4-2532/gtc n/a 31.8 — — 11 0.83 TFB1 YDR311W M95750 AAB64747.1 stan-4-2961 W19128 32.4 23.3 23 12 0.84 SPC98 YNL126W Z71402 CAA96007.1 stan-4-2821 AAC39727 30 21.5 19.9 13 0.85 BFR2 YDR299W D84656 AAB64735.1 stan-4-3108 NM_000055 42.1 20.7 22.5 14 1.05 RNA1 YMR235C Z49939 CAA90206.1 stan-4-2003/gtc CAA57714 51.5 32.1 33.7 15 1.06 GCD7 YLR291C L07116 AAB67337.1 stan-4-2913 AAC42002 52.2 34.5 35.6 16 1.27 SKI6 YGR195W L36940 CAA97221.1 stan-4-3104 BAA91279 62.5 34.8 39.1 17 1.28 NIP1 YMR309C L02899 A46417 stan-4-2825 AAD03462 42.7 30 26.7 18 1.32 LCP5 YER127W U18916 AAC03225.1 stan-4-2982 AL050003 34.7 18.6 18 19 1.63 NCE103 YNL036W Z71312 CAA95901.1 stan-4-2981 n/a 34.7 — — 20 1.67 ECO1 YFR027W D50617 BAA09266.1 stan-4-2722/gtc n/a 34.8 — — 21 1.86 ORC2 YBR060C Z35929 CAA85003,1 stan-4-3102/gtc Q13416 26.7 21 22 22 1.93 CNS1 YBR155W Z36024 CAA85114.1 stan-4-3053/gtc NP_004614 51.8 26.8 25.6 23 1.96 YPD1 YDL235C Z74283 CAA98815.1 stan-4-2907 n/a 33.3 — — 24 0.88* TIM10 YHR005C-A Z80875 AAB68435.1 stan-4-3104 NP_036588 68.1 36.6 36.6 25 1.30* SRB4 YER022W L12026 AAB64555.1 stan-4-3098 BAA88763 28.4 18 18 26

Production and Isolation of Target Proteins

[0203] The invention is also based on the generation of fungal target protein to be used in analysis as an antifungal target. Such generation requires the use of vectors comprising sequences encoding for S cerevisiae, C. albicans and/or human target proteins, in particular those listed in Table 1, cells comprising the vectors, and methods for producing the S cerevisiae, C albicans and/or human target protein homologs that involve culturing the cells.

[0204] A large number of vectors, including plasmid and fungal vectors, have been described for expression in a variety of eukaryotic and prokaryotic hosts. Such vectors will often include one or more replication systems for cloning or expression, one or more markers for selection in the host, e.g. antibiotic resistance, and one or more expression cassettes. The inserted target protein encoding sequences may be synthesized, isolated from natural sources, prepared as hybrids, etc. Ligation of the coding sequences to the transcriptional regulatory sequences may be achieved by known methods. Suitable host cells may be transformed/transfected/infected by any suitable method including electroporation, CaCl₂ mediated DNA uptake, fungal infection, microinjection, microprojectile, or other established methods.

[0205] A wide variety of host/expression vector combinations may be employed in expressing DNA sequences encoding the target proteins, in particular those listed in Table 1. Useful expression vectors, for example, may consist of segments of chromosomal, non-chromosomal and synthetic DNA sequences. Suitable vectors include derivatives of SV40 and known bacterial plasmids, e.g., E. coli plasmids col E1, pCR1, pBR322, pMa1-C2, pET, pGEX (Smith et al., Gene 67:31-40, 1988), pMB9 and their derivatives, plasmids such as RP4; phage DNAS, e.g., the numerous derivatives of phage 1, e.g., NM989, and other phage DNA, e.g., M13 and filamentous single stranded phage DNA; yeast plasmids such as the 2 micron plasmid or derivatives thereof; vectors useful in eukaryotic cells, such as vectors useful in insect or mammalian cells; vectors derived from combinations of plasmids and phage DNAs, such as plasmids that have been modified to employ phage DNA or other expression control sequences; and the like.

[0206] Appropriate host cells for expressing protein include bacteria, Archaebacteria, fungi, especially yeast, and plant and animal cells, especially mammalian cells. Of particular interest are E. coli , B. subtilis, S. cerevisiae , Sf9 cells, C129 cells, 293 cells, Neurospora, and CHO cells, COS cells, HeLa cells, and immortalized mammalian myeloid and lymphoid cell lines. Preferred replication systems include M13, Co1E1, SV40, baculovirus, lambda, adenovirus, and the like. A large number of transcription initiation and termination regulatory regions have been isolated and shown to be effective in the transcription and translation of heterologous proteins in the various hosts. Examples of these regions, methods of isolation, manner of manipulation, etc. are known in the art. Under the appropriate expression conditions, host cells can be used as a source of recombinantly produced target proteins. Advantageously, vectors may also include a promoter sequence operably linked to the S. cerevisiae, C. albicans, and/or human target protein encoding portion. The encoded S. cerevisiae, C. albicans, and/or human target protein may be expressed by using any suitable vectors and host cells, using methods disclosed or cited herein or otherwise known to those skilled in the relevant art. The particular choice of vector/host is not altogether critical to the invention.

[0207] For the purposes of this invention, the promoter sequence in the vector is bounded at its 3′ terminus by the transcription initiation site and extends upstream (5′ direction) to include the minimum number of bases or elements necessary to initiate transcription at levels detectable above background. Within the promoter sequence will be found a transcription initiation site (conveniently defined for example, by mapping with nuclease S1), as well as protein binding domains (consensus sequences) responsible for the binding of RNA polymerase.

[0208] Expression of S. cerevisiae, C. albicans, and/or human target protein may be controlled by any promoter/enhancer element known in the art, but these regulatory elements must be functional in the host selected for expression. Promoters which may be used to control S. cerevisiae, C. albicans, and/or human target protein gene expression include, but are not limited to, Cytomegalovirus immediate early promoter (CMV promoter; U.S. Pat. Nos. 5,385,839 and 5,168,062) the SV40 early promoter region (Benoist and Chambon, 1981, Nature 290:304-310), the promoter contained in the 3′ long terminal repeat of Rous sarcoma virus (Yamamoto, et al., 1980, Cell 22:787-797), the herpes thymidine kinase promoter (Wagner et al., 1981, Proc. Natl. Acad. Sci. U.S.A. 78:1441-1445), the regulatory sequences of the metallothionein gene (Brinster et al., 1982, Nature 296:39-42); prokaryotic expression vectors such as the β-lactamase promoter (Villa-Kamaroff, et al., 1978, Proc. Natl. Acad. Sci. U.S.A. 75:3727-3731), or the tac promoter (DeBoer, et al., 1983, Proc. Natl. Acad. Sci. U.S.A. 80:21-25); see also “Useful proteins from recombinant bacteria” in Scientific American, 1980, 242:74-94; promoter elements from yeast or other fungi such as the Gal 4 promoter, the ADC (alcohol dehydrogenase) promoter, PGK (phosphoglycerol kinase) promoter, alkaline phosphatase promoter; and the animal transcriptional control regions, which exhibit tissue specificity and have been utilized in transgenic animals: elastase I gene control region which is active in pancreatic acinar cells (Swift et al., 1984, Cell 38:639-646; Ornitz et al., 1986, Cold Spring Harbor Symp. Quant. Biol. 50:399-409; MacDonald, 1987, Hepatology 7:425-515); insulin gene control region which is active in pancreatic beta cells (Hanahan, 1985, Nature 315:115-122), immunoglobulin gene control region which is active in lymphoid cells (Grosschedl et al., 1984, Cell 38:647-658; Adames et al., 1985, Nature 318:533-538; Alexander et al., 1987, Mol. Cell. Biol. 7:1436-1444), mouse mammary tumor virus control region which is active in testicular, breast, lymphoid and mast cells (Leder et al., 1986, Cell 45:485-495), albumin gene control region which is active in liver (Pinkert et al., 1987, Genes and Devel. 1:268-276), alpha-fetoprotein gene control region which is active in liver (Krumlauf et al., 1985, Mol. Cell. Biol. 5:1639-1648; Hammer et al., 1987, Science 235:53-58), alpha 1-antitrypsin gene control region which is active in the liver (Kelsey et al., 1987, Genes and Devel. 1: 161-171), beta-globin gene control region which is active in myeloid cells (Mogram et al., 1985, Nature 315:338-340; Kollias et al., 1986, Cell 46:89-94), myelin basic protein gene control region which is active in oligodendrocyte cells in the brain (Readhead et al., 1987, Cell 48:703-712), myosin light chain-2 gene control region which is active in skeletal muscle (Sani, 1985, Nature 314:283-286), and gonadotropic releasing hormone gene control region which is active in the hypothalamus (Mason et al., 1986, Science 234:1372-1378).

[0209] Nucleic acids encoding wild-type or variant S. cerevisiae, C. albicans, and/or human target proteins/polypeptides may also be introduced into cells by recombination events. For example, such a sequence can be introduced into a cell, and thereby effect homologous recombination at the site of an endogenous gene or a sequence with substantial identity to the gene. Other recombination-based methods, such as non-homologous recombinations or deletion of endogenous genes by homologous recombination, may also be used.

[0210] The invention is also based on the generation of isolated and purified S. cerevisiae, C. albicans, and/or human target proteins/polypeptides, including, e.g., a polypeptide having any of the amino acid sequences depicted in Table 1, as identified by their SEQ ID NOS, as well as function-conservative variants of these polypeptides, including fragments that retain transcriptional and/or other growth regulatory activity as described above.

[0211]S. cerevisiae, C. albicans, and/or human-derived target proteins/polypeptides according to the present invention, including function-conservative variants, may be isolated from wild-type or mutant S. cerevisiae and/or C. albicans cells, respectively, or from heterologous organisms or cells (including, but not limited to, bacteria, fungi, insect, plant, and mammalian cells) into which a S. cerevisiae, C. albicans, and/or human-derived target protein-coding sequence has been introduced and expressed. Furthermore, the polypeptides may be part of recombinant fusion proteins. Alternatively, polypeptides may be chemically synthesized by commercially available automated procedures, including, without limitation, exclusive solid phase synthesis, partial solid phase methods, fragment condensation or classical solution synthesis.

[0212] “Purification” of a S. cerevisiae, C. albicans, and/or human target protein/polypeptide refers to the isolation of the polypeptide in a form that allows its transcription and/or growth regulatory activity to be measured without interference by other components of the cell in which the polypeptide is expressed. Methods for polypeptide purification are well-known in the art, including, without limitation, preparative disc-gel electrophoresis, isoelectric focusing, HPLC, reversed-phase HPLC, gel filtration, ion exchange and partition chromatography, and countercurrent distribution. For some purposes, it is preferable to produce the polypeptide in a recombinant system in which the protein contains an additional sequence tag that facilitates purification, such as, but not limited to, a polyhistidine sequence. The polypeptide can then be purified from a crude lysate of the host cell by chromatography on an appropriate solid-phase matrix. Alternatively, antibodies produced against S. cerevisiae, C. albicans, and/or human target protein or against peptides derived therefrom can be used as purification reagents. Other purification methods are possible.

[0213] The polypeptides of the present invention obtained by expression of the polynucleotides of the present invention can be purified from transformed cell cultures by methods known to those of ordinary skill in the art, such as precipitation with ammonium sulphate or ethanol, extraction under acid conditions, anion or cation exchange chromatography, hydrophobic interaction chromatography, affinity chromatography, hydroxylapatite chromatography and high performance liquid chromatography (HPLC). Techniques well-known to those of ordinary skill in the art can be used to regenerate the protein if it is denatured during its isolation or purification.

[0214] The isolated polypeptides may be modified by, for example, phosphorylation, sulfation, acylation, or other protein modifications. They may also be modified with a label capable of providing a detectable signal, i.e., a reporter molecule, either directly or indirectly, including, but not limited to, radioisotopes and fluorescent compounds.

Antibodies Directed To Target Proteins

[0215] The present invention also encompasses antibodies that bind with high affinity to the C. albicans target proteins or fragments identified as described above. As used herein, antibodies with high affinity include without limitation antibodies that bind to any C. albicans target protein identified herein in its native or denatured, i.e., folded or unfolded, conformation, particularly preferred antibodies are those which recognize either unfolded or folded target protein to be used in assays as described below. Thus, in one embodiment, the antibodies of the invention are those that are antibody preparations with high affinity for the target protein in its native conformation but not in its denatured, unfolded form, or vice versa.

[0216] Antibodies which specifically recognize a C. albicans target protein in either its native or non-native conformation, may advantageously be used in screens for potential antifungal compounds which bind or otherwise inhibit the biological activity of, the C. albicans target protein. In such a screen, antibodies specific for the C. albicans target protein in its native conformation may be used to test whether potential antifungal compounds prevent denaturation of the target protein, thus indicating a strong interaction with the target.

[0217] Following the binding of the potential antifungal compound to the C. albicans target protein, the C. albicans target protein is subjected to denaturing conditions, such as, for example, high temperature, pH, denaturing solvents, and denaturants such as, e.g., urea. Following the application of these denaturation conditions, the sample containing the C. albicans target protein and a potential antifungal compound is reacted with an antibody specific for the C. albicans target protein in either its native or non-native conformation. Binding of this antibody type indicates that the binding of the potential antifungal compounds in the screen protected the target protein from denaturation. Thus, the antibodies of the invention which are specific for either the native or the non-native target protein are useful in the screening of antifungal compounds with any C. albicans target protein.

[0218] Examples of such types of screens can be found in U.S. Pat. No. 5,585,277, issued Dec. 17, 1996, and U.S. Pat. No. 5,679,582, issued Oct. 21, 1997, each of which are incorporated herein by reference. The antibodies of the invention may be polyclonal or monoclonal, but most preferably monoclonal. The antibodies may be elicited in an animal host by immunization with a C. albicans target protein, or fragments derived therefrom which carry epitopes of the C. albicans target protein, or may be formed by in vitro immunization of immune cells. The immunogens used to elicit the antibodies may be isolated from C. albicans cells or produced in recombinant systems. The antibodies may also be produced in recombinant systems programmed with appropriate antibody-encoding DNA. Alternatively, the antibodies may be constructed by biochemical reconstitution of purified heavy and light chains. The antibodies include hybrid antibodies (i.e., containing two sets of heavy chain/light chain combinations, each of which recognizes a different antigen), chimeric antibodies (i.e., in which either the heavy chains, light chains, or both, are fusion proteins), and univalent antibodies (i.e., comprised of a heavy chain/light chain complex bound to the constant region of a second heavy chain). Also included are Fab fragments, including Fab′ and F(ab)₂ fragments of antibodies.

[0219] Methods for the production of all of the above types of antibodies and derivatives are well-known in the art and are discussed in more detail below. For example, techniques for producing and processing polyclonal antisera are disclosed in Mayer and Walker, 1987, Immunochemical Methods in Cell and Molecular Biology, Academic Press, London. Such antibodies are conveniently made using the methods and compositions disclosed in Harlow and Lane, Antibodies, A Laboratory Manual, Cold Spring Harbor Laboratory, 1988, as well as immunological and hybridoma technologies known to those of ordinary skill in the art. Where natural or synthetic peptides derived from any C. albicans target protein are used to induce an specific immune response directed against the C. albicans target protein, the peptides may be conveniently coupled to a suitable carrier such as KLH and administered in a suitable adjuvant such as Freunds. Preferably, selected peptides are coupled to a lysine core carrier substantially according to the methods of Tam (Proc. Natl. Acad. Sci. USA 1988; 85:5409).

[0220] In one embodiment, a purified recombinant C. albicans target protein is used to immunize mice, after which their spleens are removed, and splenocytes used to form cell hybrids with myeloma cells and obtain clones of antibody-secreted cells according to techniques that are standard in the art. The resulting monoclonal antibodies are screened using in vitro assays such as those described herein for binding to the C. albicans target protein or inhibiting its biological activity. The antibodies are tested for specificity of binding to the C. albicans target protein in its native conformation by screening the antibodies for target protein binding before and after subjecting the C. albicans target protein to denaturing conditions.

[0221] Antibodies specific to a target protein in an unfolded conformation are also useful in screening methods as described below.

[0222] In addition to their use in the antifungal compound screens described above, the anti-target protein antibodies of the invention, may be used to quantify a selected undenatured C. albicans target protein, using immunoassays such as, but not limited to, ELISA. The antibodies may also be used to block the native function of the chosen C. albicans target protein by inhibiting its biological activity, immunodepleting cell extracts, or interfering with other reactions related to the function of the target protein. In addition, these antibodies can be used to identify, isolate, and purify C. albicans target proteins from different sources, and to perform subcellular and histochemical localization studies as well as diagnostic analyses to determine the presence of an antigenic C. albicans target protein protein in a tissue, blood or serum sample.

Methods for Determining the Essential Nature of a Putative Essential Gene

[0223] Various methods can be used to determine whether the product of a gene is essential to the survival of a mycete or essential to the establishment or maintenance of an infection. The identification of the essential character of a gene provides additional information regarding its function and allows selection of genes for which the product constitutes a target of interest for an antifungal substance. Examples of these methods are summarized briefly below. These methods are described in the following works, each of which are hereby incorporated by reference herein: Guthrie C. and Fink G. R. (eds.), Methods in Enzymology, Vol. 194, 1991, ‘Guide to Yeast Genetics and Molecular Biology’, Academic Press Inc.; Rose A. H., A. E. Wheals and J. S. Harrison (eds.), The Yeasts, Vol. 6, 1995, ‘Yeast Genetics’, Academic Press Inc.; Ausubel F. et al. (eds.), Short Protocols in Molecular Biology, 1995, Wiley; and Brown A. J. P. and Tuite M. F. (eds.), Methods in Microbiology, Vol. 26, 1998, ‘Yeast Gene Analysis’ Academic Press Inc.

[0224] Depending on the circumstances, one of the methods described will be used, depending on the desired result. In particular, it is possible to proceed by a method of either direct inactivation of the gene or transitory inactivation of the gene. Below, we exemplify assays useful for determining the essentiality of S. cerevisiae and C. albicans genes.

S. cerevisiae Inactivation Analysis

[0225] In the yeast S. cerevisiae , the method used most generally comprises inactivation of the gene of interest at its site within the chromosome of the yeast. The wild type allele is inactivated by insertion of a genetic marker (for example a gene for auxotrophy or a resistance marker). This insertion is in general obtained by the method of gene conversion with the aid of linear deletion cassettes prepared by known methods, as described in Guthrie C. and Fink G. R. (eds.), Methods in Enzymology, or in Gultner et al. Nucleic Acid Research, 1996, 24: 2519-2524.

[0226] Preferred methods, yeast cells and vectors for determining if an S. cerevisiae gene and/or protein is essential for growth and viability are described in U.S. Provisional Patent Application 60/056,719, filed Aug. 22, 1997, U.S. patent application Ser. No. 09/138,024, filed Aug. 21, 1998, now allowed and awaiting issue, and U.S. patent application Ser. No. 09/573,322, filed May 18, 2000, each of which are incorporated herein by reference.

[0227] Briefly, an S. cerevisiae strain in which expression of a particular gene can be tightly regulated is generated. To do this the wild-type allele of the gene of interest is replaced with an allele that can be regulated by exogenous metal. The replacement is generally carried out utilizing a double-crossover strategy with a linear piece of DNA prepared by known methods as described in U.S. Patent and Application Nos. cited above.

[0228] The recombinant cells comprise, for example:

[0229] (i) a first gene encoding a transcriptional repressor protein, the expression of which has been placed under the control of a metal ion-responsive element, wherein expression of the repressor protein is stimulated by the addition of a metal ion to the growth medium of the cells;

[0230] (ii) a second gene encoding a selected target protein, wherein expression of the target protein is controlled by a promoter, the activity of which is inhibited by the repressor protein; and

[0231] (iii) a third gene encoding a biomineralization protein, wherein the third gene is inactivated and wherein inactivation of the third gene enhances the transcriptional response of the metal-responsive element to added metal ions.

[0232] In a preferred embodiment, the first gene is ROX1; the second gene is a gene encoding for a target protein described herein, controlled by an ANB1 promoter; and the third gene is SLF1.

[0233] In a particularly preferred embodiment, the recombinant cells comprise an additional gene such that the cells comprise:

[0234] (i) a first gene encoding a transcriptional repressor protein, the expression of which has been placed under the control of a metal ion-responsive element, wherein expression of the repressor protein is stimulated by the addition of a metal ion to the growth medium of the cells;

[0235] (ii) a second gene encoding a target protein, wherein expression of the target protein is controlled by a promoter, the activity of which is inhibited by the repressor protein;

[0236] (iii) a third gene encoding a protein that targets ubiquitin-containing polypeptides for degradation, the expression of which has been placed under the control of a metal ion-responsive element, wherein expression of the ubiquitin targeting protein is stimulated by the addition of a metal ion to the growth medium of the cells, wherein the stability of the target protein is controlled by the ubiquitin targeting protein; and

[0237] (iv) a fourth gene encoding a biomineralization protein, wherein the fourth gene is inactivated and wherein inactivation of the fourth gene enhances the transcriptional response of the metal-responsive element to added metal ions.

[0238] Thus, in a particularly preferred embodiment, the first gene is ROX1; the second gene, encoding for a target protein according to the invention, is controlled by an ANB1 promoter; the third gene is UBR1; and the fourth gene is SLF1.

[0239] Utilizing this preferred system, expression of the target protein gene is carried out in the absence of added metal ion. When it is desired to decrease or eliminate expression of the target protein gene, metal ions are added to the medium, which stimulate expression of the repressor and ubiquitin tarteting protein to a degree that is dependent upon the concentration of added metal ions and represses transcription of the target protein gene and reduces the stability of the protein. In the preferred system, expression of Rox1 and Ubr1 protein is induced by the addition of copper to the growth media, and thus, expression of the target protein is shut off. If the engineered S. cerevisiae strain containing the target protein gene under control of this repressible system stops growing and loses viability in the presence of copper, the target protein is shown to be essential and a cidal target.

[0240]S. cerevisiae inactivation analyses of the target proteins described in Table 1 were conducted as described herein and in Example 1, and the results are presented in FIGS. 27-52.

[0241] Once the S. cerevisiae target protein has been shown to be both essential for growth and viability, and a cidal target in S. cerevisiae , the homologous C. albicans gene and or protein must then be analyzed to determine if either are essential for growth and can act as a potential cidal target in C. albicans. The C. albicans gene is identified by comparative sequence analysis. When a DNA fragment is required for some type of analysis (gene inactivation or protein expression) it is preferably obtained by PCR cloning using methods well known in the art (See for example, Eds. C. W. Dieffenbach and E. F. Dvekfler, PCR Primer:A Laboratory Manual Cold Spring Harbor Laboratory Press, Plainview, N.Y., 1995.)

C. albicans Deletion Analysis

[0242] Determining if a particular gene or protein is essential for growth is carried out by determining if, when the gene or protein is inactivated in C. albicans, the cells will survive. Because C. albicans is a diploid fungus which, largely due to the absence of a sexual phase in its life cycle, is resistant to a considerable number of genetic techniques that are applicable to S. cerevisiae, DNA constructs are used to inactivate, or delete all, or a portion, of the gene of interest in C. albicans. Such constructs provide for the inactivation or deletion of the wild type allele by insertion of a genetic selection marker (for example a gene for auxotrophy or a resistance marker). This insertion is in general obtained by the method of gene conversion with the aid of linear deletion cassettes prepared by known methods of DNA manipulation as described above.

[0243] In one embodiment, in order to assess whether the target protein gene is essential for growth in C. albicans, plasmids can be used to construct a double disruptant strain according to the methods outlined in FIGS. 53-78. If a double disruptant strain can be produces, then the gene is determined to be non-essential. Methods used in these constructions employ common techniques employed in the genetic manipulation and screening of C. albicans.

[0244] One commonly used approach utilizes C. albicans strain CAI4 (Fonzi and Irwin, 1993) to generate a uridine auxotrophic strain of C. albicans transformed with linearized DNA fragments containing the Ca URA3 gene (able to confer uridine prototrophy upon transformants) flanked by identical HisG sequences. This HisG-CaURA3-HisG cassette is flanked by sequences upstream of the gene of interest on one side and downstream of it on the other side.

[0245] Prototrophic transformants have undergone replacement of one copy of the gene of interest with the HisG-CaURA3-HisG cassette. Auxotrophic, uridine requiring derivatives can be isolated by selecting for 5′ fluoro-orotic acid (FOA) resistance in the presence of uridine. The URA3 gene product converts FOA into fluorouracil which is toxic. FOA selection therefore allows one to select cells that have lost the URA3 gene upon cis-recombination of the two identical hisG flanking regions.

[0246] To determine if the gene of interest is essential for growth, a second disruption plasmid is used in order to attempt to inactivate the second copy of the gene. The CaURA3 gene, as described above, is able to confer uridine prototrophy upon transformants, and is flanked by identical HisG sequences. This HisG-CaURA3-HisG cassette is flanked by sequences upstream of the gene of interest on one side and downstream of the gene of interest on the other side. Generation of prototrophic transformants can occur by integration of the cassette into the non-disrupted allele of the gene of interest, by replacement of the hisG cassette with the CaURA3 cassette, or by non-homologous recombination events. Transformants that disrupt the second copy of the gene is proof that the gene of interest is not essential. In order to establish that a gene in C. albicans is essential for growth, at least 20 second round transformants should be analyzed. If analysis of 20 transformants demonstrates that the second copy of the gene is still present, this indicates that the gene is essential. All transformants are analyzed by Southern blotting. Candida albicans transformations are performed as described (Elble R., Biotechniques 1992; 13:18-20).

[0247] A second commonly used approach utilizes C. albicans strain CAI8 (Fonzi and Irwin, 1993). CAI8 is a uridine and adenine auxotrohic strain that can be converted to uridine and adenine prototophy by transformation with C. albicans URA3 (CaURA3) and C. albicans ADE2 (CaADE2), respectively.

[0248] Deletion of the first allele of the gene of interest is accomplished by transformation of CAI8 to adenine prototophy with a linearized DNA fragment containing the CaADE2 gene flanked by sequences upstream of the gene of interest on one site and downstream of it on the other site.

[0249] To determine if the gene of interest is essential for growth, a second disruption plasmid is used in order to attempt to inactivate the second copy of the gene. The CaURA3 is flanked by sequences upstream of the gene of interest on one site and downstream of it on the other site. Generation of adenine/uridine prototrophic transformants can occur by integration of the cassette into the non-disrupted allele of the gene of interest, or by non-homologous recombination events.. Transformants that disrupt the second copy of the gene is proof that the gene of interest is not essential. In order to establish that a gene in C. albicans is essential for growth at least 20 second round transformants should be analyzed. If analysis of 20 transformants shows that the second copy of the gene is still present and could not be deleted, which indicates that the gene is essential. All transformants are analyzed by Southern blotting. Candida albicans transformations are performed as previously described (Elble, 1992).

[0250] URA3 can be used for either of the selectable markers as described above with the CAI8 strain.

[0251] These types of analytical procedures can also be carried out by transitory inactivation of the gene of interest with adjustable promoters other than that described above with the Rox1 repressor protein. To achieve this, the native promoter of the gene is replaced by an adjustable promoter directly on the chromosome or on an extra chromosomal plasmid. One example of another adjustable promoter for use in this method is the CAL promoter or its derivatives, or the tetO promoter (Mumberg et al. 1994, Nucleic Acid Research, 22: 5767-5768; Belli et al. 1998, Yeast, 14: 1127-1138). The essential character of the gene studied can thus be observed, while the promoter used is repressed, either in the haploid strains in the yeast S. cerevisiae, or after inactivation of the second allele in the diploid microorganism (for example C. albicans ).

[0252]C. albicans deletion analyses were carried out for each of the target genes identified in Table 1, as described in this section and in Example 2. The results are presented in FIGS. 53-78, each figure representing a single target gene.

Methods for Identifying Homologous Genes

[0253] From a known essential gene in a species, genes which are homologous or have the same function in another species of mycete can be identified. The methods known to those of ordinary skill in the art can be used to identify a homolog to a gene studied in another species of mycete (so-called “orthologous” genes) or genes having the same function as the gene studied. Examples of methods which can be used are given below. These methods are described in the following works which are hereby incorporated by reference herein: Sambrook et al. 1989, Molecular Cloning, Cold Spring Harbor Laboratory Press; Ausubel F. et al. eds. Short Protocols in Molecular Biology, 1995, Wiley; and Guthrie C. and Fink G. R. eds. Methods in Enzymology, Vol. 194, 1991, ‘Guide to Yeast Genetics and Molecular Biology’, Academic Press Inc.

[0254] Such methods include screening for homology or gene complementation to genomic or cDNA libraries of pathogenic mycetes, or PCR amplification of such library DNA using specific primers selected by virtue of their homology to the nucleotide sequence of interest.

[0255] The homologous DNA sequences of other mycetes as defined above can be isolated, in particular, by the PCR amplification methods known to those of ordinary skill in the art. A non-limiting of such PCR technique is carried out using degenerate nucleotide primers to amplify these homologous DNAs from genomic or cDNA libraries of the corresponding mycetes. The cDNAs can also be prepared from mRNAs isolated from mycetes of various species studied in the context of the present invention, directed to Saccharomyces cerevisiae and Candida albicans, namely Candida stellatoidea, Candida tropicalis, Candida parapsilosis, Candida krusei, Candida pseudotropicalis, Candida quillennondii, Candida glabrata, Candida lusianiae or Candida rugosa, or also mycetes of the type Aspergillus or Cryptococcus, and in particular, for example, Aspergillus fumigatus, Coccidioides immitis, Cryptococcus neoformans, Histoplasma capsulatum, Blastomyces dermatitidis, Paracoccidioides brasiliens and Sporothrix schenckil, or also mycetes of the classes of Phycomycetes or Eumycetes, in particular the sub-classes of Basidiomycetes, Ascomycetes, Mehiascomycetales (yeast) and Plectascales, Gymnascales (fungus of the skin and hair) or of the class of Hyphomycetes, in particular the sub-classes Conidiosporales and Thallosporales, and among these the following species: Mucor, Rhizopus, Coccidioides, Paracoccidioides (Blastomyces, brasiliensis), Endomyces (Blastomyces), Aspergillus, Menicilium. (Scopulariopsis), Trichophyton (Ctenomyces), Epidermophton, Microsporon, Piedraia, Hormodendron, Phialophora, Sporotrichon, Cryptococcus, Candida, Geotrichum, Trichosporon or also Toropsulosis.

[0256] Homologous polynucleotides can thus be obtained using the usual methods of cloning and screening, such as those of cloning and sequencing from fragments of chromosomal DNA extracted from cells. For example, to obtain such homologous polynucleotides, it is possible to start from a library of chromosomal DNA fragments. A probe corresponding to a radiolabeled oligonucleotide, preferably made up of 17 nucleotides or more and derived from a partial sequence, can be prepared. The clones containing a DNA identical to that of the probe can thus be identified under stringent conditions. By sequencing individual clones identified in this way using sequencing primers resulting from the original sequence, it is then possible to prolong the sequence in both directions to determine the sequence of the complete gene. Such sequencing can usually be carried out effectively using a double-stranded denatured DNA prepared from a plasmid. Such techniques are described by Maniatis, T., Frisch, E. F., and Sambrook as indicated above. (Laboratory Manual, Cold Spring Harbor, N.Y. (1989), in particular in 1.90 and 13.70 in the chapters on screening by hybridization and sequencing from double-stranded denatured DNA).

[0257] The genomic DNA or cDNA libraries can be prepared by known methods and the polynucleotide fragments obtained are integrated into an expression vector, for example a vector such as pRS423 or its derivatives, which can be used both in the bacterium E. coli and in S. cerevisiae. Screening of the library will be carried out by conventional methods of in situ hybridization on a replica of bacterial colonies. The hybridization conditions will be adapted to the stringency required for the reaction so that fragments more or less homologous with the gene studied are identified. The genes of other species of mycetes can also be identified by known so-called “gene complementation” methods. For example, a strain of S. cerevisiae in which an identified essential gene has been placed under the control of an adjustable promoter can be transformed by a representative sample of a DNA or cDNA library corresponding to the mycete studied. When yeasts are cultured under conditions such that the promoter is repressed, the only yeasts that can survive are the ones that carry a recombinant vector containing a sequence of the mycete studied which is functionally equivalent to the initial essential gene. The gene sequence in the mycete studied is then identified by isolating the recombinant vector and sequencing it by known methods. In the same way, the so called “plasmid shuffle” method allows selection of yeasts which have lost expression of the initial essential gene and contain a functionally equivalent sequence originating from another mycete.

[0258] This type of study can be performed on various species: the genes which are functionally equivalent or homologous in sequence to an essential gene can be isolated in other mycetes, and in particular in the various mycetes which are pathogenic to humans. For this, it is possible to use, in particular, mycetes belonging to the classes Zygomycetes, Basidiomycetes, Ascomycetes and Deuteromycetes. More particularly, the mycetes will belong to the sub-classes Candida spp., in particular Candida albicans, Candida glabrata, Candida tropicalis, Candida parapsilosis and Candida krusei. The mycetes will also belong to the sub-classes Aspergillus fumigatus, Coccidioides immitis, Cryptococcus neofonnans, Histoplasma capsulatum, Blastomyces dermatidis, Paracoccidioidesbrasiliensis and Sprorothrix schenckii.

Inhibition of Fungal Growth

[0259] The present invention provides for a number of strategies to inhibit fungal growth by inhibiting the biological activity of the target proteins provided herein. As described above, these fungal target proteins are involved in a wide range of activities related to growth and viability, such as, but not limited to, DNA transcription, mRNA translation, mRNA and protein processing and trasport, cell division, growth regulation, cell cycle regulation, and other processes. Although the exact function of some target proteins is not yet known, the target proteins provided by the invention all have the common feature of being involved in fungal growth. In the section below, transcription is exemplified as one potential mechanism through which growth can be affected, but it is to be understood that other mechanisms not specifically described below can be used for studying and/or implementing growth inhibition using the methods described herein.

Transcription

[0260] The present invention provides methods of modifying gene transcription by contacting a S. cerevisiae and/or C. albicans target protein with substances that bind to, or interact with, such a protein or the DNA/RNA encoding such a protein. These substances may modify the influence of the S. cerevisiae and/or C. albicans target protein on transcription, chromatin remodeling or other processes essential to gene transcription. Substances that bind to, or interact with, the S. cerevisiae and/or C. albicans target protein or the DNA/RNA encoding such a protein can prevent or enhance its biological activity, which may directly or indirectly inhibit fungal growth.

[0261] For example, anti-sense or non-sense nucleotide sequences that hybridize with the S. cerevisiae and/or C. albicans target protein DNA or RNA and either completely inhibit or decrease their translation or transcription can prevent and inhibit the transcription of other fungal genes. Alternatively, compounds that can bind to or interact with the S. cerevisiae and/or C. albicans target protein can prevent or enhance the function of the protein in the transcription process. These substances include antibodies that are reactive with and bind to either or both of the S. cerevisiae and/or C. albicans target proteins.

Candidate Inhibitors

[0262] Once it has been determined that the target protein is a cidal target in Saccharomyces cerevisiae and essential for growth Candida albicans, the protein may be used as a cidal target in order to isolate candidate inhibitors of fungal growth and/or infection.

[0263] As noted above, a “candidate inhibitor,” as used herein, is any compound with a potential to inhibit, in Candida albicans or other fungal species, the biological activity of a target protein. Candidate inhibitor compounds are first identified in a primary screen against the C. albicans target protein. This primary screen may be affinity based, mechanistic (e.g., in vitro transcription assay), or cell-based (e.g., reporter assay). Such assays are described further below. A candidate inhibitor is tested in a concentration range that depends upon the molecular weight of the molecule and the type of assay. For example, for inhibition of protein/protein or protein/DNA complex formation or transcription elongation small molecules (as defined below) may be tested in a concentration range of 1 pg - 100 ug/mL, preferably at about 100 pg -20 ug/mL; large molecules, e.g., peptides, may be tested in the range of 10 ng -100 ug/mL, preferably 100 ng -10 ug/mL.

[0264] Inhibitors of Candida albicans growth or viability may target the C. albicans target proteins described herein, or it may target a protein or nucleic acid that interacts with the C. albicans target protein to prevent the natural biological interaction that occurs in vivo. An inhibitor identified as described herein must possess the property that at some concentration it will inhibit Candida albicans growth or viability, most preferably at the same concentration it will not significantly affect the growth of mammalian, particularly human, cells.

[0265] Candidate inhibitors include peptide and polypeptide inhibitors having an amino acid sequence based upon the C. albicans target protein sequences described herein. For example, a fragment of the C. albicans target protein may act to prevent the growth of wild type Candida albicans cells because it acts as a competitive inhibitor with respect to the C. albicans target protein binding to other proteins involved in Candida growth, e.g., chromatin binding, cell division, transcription, or another essential activity.

[0266] Inhibitory compounds to be tested are screened from large libraries of synthetic or natural compounds. Numerous means are currently used for random and directed synthesis of saccharide, peptide, and nucleic acid based compounds. Synthetic compound libraries are commercially available from Maybridge Chemical Co. (Trevillet, Cornwall, UK), Comgenex (Princeton, N.J.), Brandon Associates (Merrimack, N.H.), and Microsource (New Milford, Conn.). A rare chemical library is available from Aldrich (Milwaukee, Wis.). Alternatively, libraries of natural compounds in the form of bacterial, fungal, plant and animal extracts are available from e.g. Pan Laboratories (Bothell, Wash.) or MycoSearch (N.C.), or are readily producible. Additionally, natural and synthetically produced libraries and compounds are readily modified through conventional chemical, physical, and biochemical means.

[0267] Compounds useful as inhibitors may be found within numerous chemical classes, though typically they are organic compounds, and preferably small organic compounds. Small organic compounds have a molecular weight of more than 50 yet less than about 2,500 daltons, preferably less than about 750, more preferably less than about 350 daltons. Exemplary classes include heterocycles, peptides, saccharides, steroids, and the like. The compounds may be modified to enhance efficacy, stability, pharmaceutical compatibility, and the like. Structural identification of an agent may be used to identify, generate, or screen additional agents. For example, where peptide agents are identified, they may be modified in a variety of ways to enhance their stability, such as using an unnatural amino acid, such as a D-amino acid, particularly D-alanine, by functionalizing the amino or carboxylic terminus, e.g. for the amino group, acylation or alkylation, and for the carboxyl group, esterification or amidification, or the like. Other methods of stabilization may include encapsulation, for example, in liposomes, etc.

Primary Inhibitor Screening High-Throughput Methods For Screening Inhibitors

[0268] In a preferred embodiment, a high-throughput screening protocol, also referred to as ATLAS, is used to survey a large number of test compounds for their ability to bind or otherwise interact with a C. albicans target protein. High-throughput screening methods are described in U.S. Pat. Nos. 5,585,277 and 5,679,582, in U.S. Ser. No. 08/547,889, and in the published PCT application PCT/US96/19698, and may be used for identifying a ligand that binds the target proteins described herein. According to these methods, a ligand, or a plurality of ligands for a C. albicans target protein is identified by its ability to influence the extent of folding or the rate of folding or unfolding of the target protein. Experimental conditions are chosen so that the target protein unfolds to a measurable extent, whether reversible or irreversible. If the test ligand binds to the target protein under these conditions, the relative amount of folded:unfolded target protein or the rate of folding or unfolding of the target protein in the presence of the test ligand will be different, i.e. higher or lower, than that observed in the absence of the test ligand. Thus, the method encompasses incubating the C. albicans target protein in the presence and absence of a plurality of test ligands under conditions in which (in the absence of ligand) the target protein would partially or totally unfold. This is followed by analysis of the absolute or relative amounts of folded vs. unfolded target protein or of the rate of folding or unfolding of the target protein.

[0269] An important feature of this method is that it will detect any compound that binds to any sequence or domain of the C. albicans target protein, and not only to sequences or domains that are intimately involved in a biological activity or function. The binding sequence, region, or domain may be present on the surface of the target protein when it is in its folded state, or may be buried in the interior of the protein. Some binding sites may only become accessible to ligand binding when the protein is partially or totally unfolded.

[0270] Briefly, to carry out this method, the test ligand or ligands are combined with the C. albicans target protein, and the mixture is maintained under appropriate conditions and for a sufficient time to allow binding of the test ligand. Experimental conditions are determined empirically. When testing test ligands, incubation conditions are chosen so that most ligand:target protein interactions would be expected to proceed to completion. The test ligand is present in molar excess relative to the target protein. The target protein can be in a soluble form, or, alternatively, can be bound to a solid phase matrix. The matrix may comprise without limitation beads, membrane filters, plastic surfaces, or other suitable solid supports.

[0271] In a preferred embodiment, binding of test ligand or ligands to the target protein is detected through the use of proteolysis. This assay is based on the increased susceptibility of unfolded, denatured polypeptides to protease digestion relative to that of folded proteins. In this case, the test ligand-target protein combination, and a control combination lacking the test ligand, are treated with one or more proteases that act preferentially upon unfolded target protein. After an appropriate period of incubation, the level of intact i.e. unproteolysed target protein is assessed using one of the methods described below e.g. gel electrophoresis and/or inmunoassay.

[0272] There are two possible outcomes that indicate that the test ligand has bound the target protein. Either 1) a significantly higher, or 2) a significantly lower absolute amount of intact or degraded protein may be observed in the presence of ligand than in its absence.

[0273] Proteases useful in practicing the present invention include without limitation trypsin, chymotrypsin, V8 protease, elastase, carboxypeptidase, proteinase K, thermolysin, papain and subtilisin (all of which can be obtained from Sigma Chemical Co., St. Louis, Mo.). The most important criterion in, selecting a protease or proteases for use in practicing the present invention is that the protease(s) must be capable of digesting the target protein under the chosen incubation conditions, and that this activity be preferentially directed towards the unfolded form of the protein. To avoid “false positive” results caused by test ligands that directly inhibit the protease, more than one protease, particularly proteases with different enzymatic mechanisms of action, can be used simultaneously or in parallel assays. In addition, co-factors that are required for the activity of the protease(s) are provided in excess, to avoid false positive results due to test ligands that may sequester these factors.

[0274] In a typical embodiment of this method, purified target protein is first taken up to a final concentration of about 1-100 g/mL in a buffer containing 50 mM Tris-HCl, pH 7.5, 10% DMSO, 50 mM NaCl, 10% glycerol, and 1.0 mM DTT. Proteases, such as, for example, proteinase K or thermolysin (proteases with distinct mechanisms of action), are then added individually to a final concentration of 0.2-10.0 g/mL. Parallel incubations are performed for different time periods ranging from 5 minutes to one hour, preferably 30 minutes, at 4° C., 15° C., 25° C., and 35° C. Reactions are terminated by addition of an appropriate protease inhibitor, such as, for example, phenylmethylsulfonyl chloride (PMSF) to a final concentration of 1 mM (for serine proteases), ethylenediaminotetraacetic acid (EDTA) to a final concentration of 20 mM (for metalloproteases), or iodoacetamide (for cysteine proteases). The amount of intact protein remaining in the reaction mixture at the end of the incubation period may then be assessed by any method, including without limitation polyacrylamide gel electrophoresis, ELISA, or binding to nitrocellulose filters. It will be understood that additional experiments employing a narrower range of temperatures can be performed to establish appropriate conditions. This protocol allows the selection of appropriate conditions (e.g., protease concentration and digestion temperature) that result in digestion of approximately 70% of the target protein within a 30 minute incubation period, indicating that a significant degree of unfolding has occurred.

[0275] In another embodiment, the relative amount of folded and unfolded target protein in the presence and absence of test ligand is assessed by measuring the relative amount of the protein that binds to an appropriate surface. This method takes advantage of the increased propensity of unfolded proteins to adhere to surfaces, which is due to the increased surface area, and decrease in masking of hydrophobic residues, that results from unfolding. If a test ligand binds the C. albicans target protein (i.e., is a ligand), it may stabilize the folded form of the target protein and decrease its binding to a solid surface. Alternatively, a ligand may stabilize the unfolded form of the protein and increase its binding to a solid surface.

[0276] Surfaces suitable for this purpose include without limitation microtiter plates constructed from a variety of treated or untreated plastics, plates treated for tissue culture or for high protein binding, nitrocellulose filters and PVDF filters.

[0277] In another embodiment, the extent to which folded and unfolded target protein are present in the test combination is assessed through the use of antibodies specific for either the unfolded state or the folded state of the protein i.e. denatured-specific (“DS”), or native-specific (“NS”) antibodies, respectively. (Breyer, J. Biol. Chem. 1989; 264(5):13348-13354). Polyclonal or monoclonal antibodies are prepared as described above. The resulting antibodies are screened for preferential binding to the C. albicans target protein in its denatured state. These antibodies are used to screen for inhibitors of these interactions.

[0278] In another embodiment, molecular chaperones are used to assess the relative levels of folded and unfolded protein in a test combination. Chaperones encompass known proteins that bind unfolded proteins as part of their normal physiological function. In this embodiment, a test combination containing the test ligand and the C. albicans target protein is exposed to a solid support e.g. microtiter plate or other suitable surface coated with a molecular chaperone, under conditions appropriate for binding the target protein with its ligand and binding of the molecular chaperone to unfolded target protein. The unfolded target protein in the solution will have a greater tendency to bind to the molecular chaperone-covered surface relative to the ligand-stabilized folded target protein. Thus, the ability of the test ligand to bind target protein can be determined by determining the amount of target protein remaining unbound, or the amount bound to the chaperone-coated surface. Alternatively, a competition assay for binding to molecular chaperones can be utilized.

[0279] Once conditions are established for high-throughput screening as described above, the protocol is repeated simultaneously with a large number of test ligands at concentrations ranging from, e.g., 20 to 200 M. Observation of at least a two-fold increase or decrease in the extent of digestion of the target protein signifies a “hit” compound, i.e., a ligand that binds the target protein. Preferred conditions are those in which between 0.1% and 1% of test ligands are identified as “hit” compounds using this procedure.

[0280] In yet another embodiment, the test and control combinations described above can be contacted with a conformation-sensitive probe containing a reporter molecule such as, e.g., a fluorescent molecule or radionucleotide, i.e., a probe that binds preferentially to the folded, unfolded, or molten globule state of the C. albicans target protein or whose reporter-mediated properties are in any way affected by the folding status of the C. albicans target protein.

Phase Display Technology Screening

[0281] In addition to the high-throughput screening techniques described above, technologies for molecular identification can be employed in the identification of inhibitor molecules. One of these technologies is phage display technology (U.S. Pat. No. 5,403,484. Viruses Expressing Chimeric Binding Proteins). Phage display permits identification of a binding protein against a chosen target. Phage display is a protocol of molecular screening which utilizes recombinant bacteriophage. The technology involves transforming bacteriophage with a gene that encodes an appropriate ligand (in this case, a candidate inhibitor) capable of binding to the target molecule of interest. For the purposes of this disclosure, the target molecule may be a C. albicans target protein. The transformed bacteriophage (which preferably is tethered to a solid support) express the candidate inhibitor and display it on their phage coat. The cells or viruses bearing the candidate inhibitor which recognize the target molecule are isolated and amplified. The successful inhibitors are then characterized.

[0282] Phage display technology has advantages over standard affinity ligand screening technologies. The phage surface displays the microprotein ligand in a three dimensional conformation, more closely resembling its naturally occurring conformation. This allows for more specific and higher affinity binding for screening purposes.

Biospecific Interaction Analysis Screening

[0283] Another relatively new screening technology which may be applied to the inhibitor screening assays of this invention is biospecific interaction analysis (BIAcore, Pharmacia Biosensor AB, Uppsala, Sweden). This technology is described in detail by Jonsson et al. (Biotechniques 11:5, 620-627 (1991)). Biospecific interaction analysis utilizes surface plasmon resonance (SPR) to monitor the adsorption of biomolecular complexes on a sensor chip. SPR measures the changes in refractive index of a polarized light directed at the surface of the sensor chip.

[0284] Specific ligands (i.e., candidate inhibitors) capable of binding to the target molecule of interest (i.e., a C. albicans target protein or a protein-protein or protein-DNA complex containing the C. albicans target protein) are immobilized to the sensor chip. In the presence of the target molecule, specific binding to the immobilized ligand occurs. The nascent immobilized ligand-target molecule complex causes a change in the refractive index of the polarized light and is detected on a diode array. Biospecific interaction analysis provides the advantages of; 1) allowing for label-free studies of molecular complex formation; 2) studying molecular interactions in real time as the assay is passed over the sensor chip; 3) detecting surface concentrations down to 10 pg/mm²; detecting interactions between two or more molecules; and 4) being fully automated (Biotechniques 11:5, 620-627 (1991)).

Screening Through Use Of A Transcription Assay

[0285] In cases where the target protein has been identified as being required for transcription per se and/or elongation, the present invention encompasses the identification of agents useful in modulating fungal gene transcription, particularly the transcription of genes by RNA polymerase II in a target protein-dependent manner. Thus, if the target protein has been identified as being essential for transcription and/or elongation, inhibitors of Candida albicans growth and viability may also be screened either by measuring inhibition of any of the activities described above, or by assaying formation of a protein/DNA complex or inhibition of sporulation when cells are contacted with Candida albicans inhibitors.

In Vitro Transcription Assay

[0286] If an essential target protein has been identified as being required for transcription, and it has been identified according to any of the screening methods described above, its activity and effect on transcription can be confirmed by adding it to an in vitro transcription reaction, and measuring its effect on the target protein-mediated activated transcription, using an in vitro transcription assay. For example, DNA of interest (i.e., DNA to be transcribed) can be admixed with (i) purified RNA polymerase II, (ii) the SRB proteins, (iii) transcription factors b, e, g or a, (iv) the C. albicans target protein and (v) the substance (ligand) to be tested. The mixture is maintained under conditions sufficient for transcription to occur. The resulting combination is referred to as a test mixture. DNA transcription can be assessed by determining the quantity of mRNA produced. Transcription is determined in the presence of the substance being tested and compared to DNA transcription in the absence of the test substance taking place under identical conditions (e.g., a control mixture). If transcription occurs to a lesser extent in the test mixture, (i.e., in the presence of the substance being evaluated) than in the control mixture, the substance may have interacted with one or more SRB proteins , or with the C. albicans target protein, preferably in such a manner as to inhibit transcription. If transcription occurs to a greater extent in the test mixture than in the control mixture, the substance has interacted in such a manner as to stimulate transcription.

[0287] Transcription of DNA sequences, or translation of mRNA sequences encoding the C. albicans target protein can also be inhibited or decreased by inhibitor compounds, resulting in decreased production of, or the complete absence of the C. albicans target protein. Gene transcription can be modified by introducing an effective amount of a substance into a cell that inhibits transcription of the gene encoding the C. albicans target protein, or that inhibits translation of mRNA encoding the C. albicans target protein. For example, antisense nucleotide sequences can be introduced into the cell that will hybridize with the gene encoding the target protein and inhibit transcription of the gene. (See, Current Protocols in Molecular Biology, Eds. Ausubel et al. Greene Publ. Assoc., Wiley-Interscience, NY, N.Y., 1997). Alternatively, an antisense sequence can be introduced into the cell that will interfere with translation of the mRNA encoding the C. albicans target protein.

Secondary Screens—Measurement of Inhibition of Candida albicans Growth in Culture

[0288] Once a putative inhibitor has been identified in the primary screen or screens, it may be desirable to determine the effect of the inhibitor on the growth and/or viability of Candida albicans in culture. Methods for performing tests on fungal growth inhibition in culture are well-known in the art.

[0289] Non-limiting examples of such procedures test the candidate inhibitor compounds for antifungal activity against a panel of three strains: C. albicans, S. cerevisiae , and A. nidulans. One such procedure is based on the NCCLS M27A method (The National Committee for Clinical Laboratory Standards, Reference Method for Broth Microdilution Antifungal Susceptibility Testing of Yeasts; approved standard, 1997) to measure minimum inhibitory concentrations (MICs) and minimum fungicidal concentrations (MFCs). An overview of this of this protocol follows.

Media

[0290] 1 . Sabouraud dextrose agar (SDA): 10 g Bacto Neopeptone; 40 g Bacto Dextrose; 15 g Bacto Agar. Suspend contents in 1 liter of water and boil while stirring to dissolve completely. Autoclave for 15 minutes. SDA is conveniently sold as a powdered mix by DIFCO (Cat #0109-17-1).

[0291] 2. Potato dextrose agar (PDA): 4 g Potato extract; 20 g Bacto Dextrose; 15 g Bacto Agar. Suspend contents in 1 liter of water and boil while stirring to dissolve completely. Autoclave for 15 minutes. PDA is conveniently sold as a powdered mix by DIFCO (Cat #0013-17-6).

[0292] 3. RPMI-1640: 10.4 g powdered media (Sigma R-6504, w/ glutamine & w/o bicarbonate); 2.0 g NaHCO₃ (Sigma S-6297); 34.53 g MOPS buffer (Sigma M-6270). Dissolve powdered media and NaHCO₃ in 900 ml distilled water. Add MOPS and stir until dissolved. Adjust pH to 7.0 using 1N NaOH. Bring final volume to 1 liter, filter sterilize, and store at 4° C.

[0293] 4. RPMI-1640 with 12.5% mouse serum: 10.4 g powdered media (Sigma R-6504, w/ glutamine & w/o bicarbonate); 2.0 g NaHCO₃ (Sigma S-6297); 34.53 g MOPS buffer (Sigma M-6270); 50 ml mouse serum (Sigma S-7273). Dissolve powdered media and NaHCO₃ in 750 ml distilled water. Add MOPS and stir until dissolved. Adjust pH to 7.0 using 1N NaOH and bring volume to 875 ml. Remove 350 ml and add to it 50 ml of mouse serum. Bring remaining volume of media (525 ml) to 600 ml with the addition of 75 ml of distilled water. Filter sterilize each solution and store at 4° C.

Inoculum Preparation

[0294] 1. Yeasts: Yeasts (Saccharonyces cerevisiae and Candida albicans) are cultured on Sabouraud dextrose agar (SDA) plates in a 35° C. incubator. Strains on SDA plates are stored at 4° C. and used as working stock cultures. Working stock plates are prepared once a month from frozen stocks of cells. Inoculum for susceptibility testing is prepared from fresh 24 hour cultures. 5-10 colonies are scraped from the plate and suspended in three milliliters of sterile 0.85% saline (8.5 g/liter NaCl). The cell density of the solution is determined by measuring the absorbance in a spectrophotometer (Shimadzu UV-1201S UV-VIS Spectrophotometer) set at 600 nm. An absorbance value between 0.1 and 0.4 is required for an accurate reading.

[0295] For C. albicans, e.g., strain ATCC 10231, 1.0 OD₆₀₀ unit is approximately 10⁷ cells per ml while for Saccharomyces cerevisiae strain CTY552 1.0 OD₆₀₀ unit is slightly less than 10⁷ cells per ml. Dilute the cell suspension with the appropriate medium (typically RPMI-1640) to OD₆₀₀=0.0003 for Candida and OD600=0.0004 for Saccharomyces. The diluted suspension should contain approximately 3×10³ cells per ml (this is a 2× concentration inoculum). Two 100 ul aliquots of this dilution should be spread on SDA plates and incubated at 35° C. for 1-2 days to determine the precise number of colony forming units. An acceptable range for the inoculum (2×) is 1-5×10³ cfu/ml (100-500 for 100 ul). Following two-fold dilution of the inoculum with compound, the final concentration of cells will be 0.5-2.5×10³ per ml. The inoculum should be kept at 4° C. and used within a few hours.

[0296] 2. Filamentous fungi: Filamentous fungi (Aspergillus spp.) should be cultured on Potato dextrose agar (PDA) plates in a 35° C. incubator. A fresh plate should be started from frozen cell stocks once a month. Inoculum of Aspergillus for susceptibility testing is prepared from plates incubated at 35° C. for 5 days. Colonies are covered with five ml of sterile 0.85% saline (8.5 g/liter NaCl) and gently rocked for 10-15 minutes. To dislodge the conidia, use an automatic pipettor to gently wash over the colonies. The saline solution is removed from the plate and the heavy particles allowed to settle for 3-5 minutes. The upper suspension is removed and vortexed for 15 sec. The turbidity of the solution is determined by measuring the absorbance in a spectrophotometer (Shimadzu UV-1201S UV-VIS Spectrophotometer) set at 600 nm. An absorbance value between 0.1 and 0.4 is required for an accurate reading.

[0297] Dilute the cell suspension with the appropriate medium (typically RPMI-1640) to OD₆₀₀=0.0004. The final suspension should contain approximately 3×103 cfu per ml (this is a 2× concentration inoculum). Two 100 ul aliquots of this dilution should be spread on SDA plates and incubated at 35° C. for 1-2 days to determine the precise number of colony forming units. An acceptable range for the inoculum (2×) is 1-5×10³ cfu/ml (100-500 for 100 ul). Following two-fold dilution of the inoculum with compound, the final concentration of cells will be 0.5-2.5×10³ per ml. The inoculum should be kept at 4° C. and used within a few hours.

Compound Preparation

[0298] Stock solutions and concentrations tested will vary from compound to compound. In general, though, stock solutions of 12.8 mg/ml in DMSO (Sigma D-8779) should be prepared. This will allow for a 128 ug/ml starting test concentration containing 1% DMSO. Stock solutions should be stored at −20° C. and dilutions for antifungal testing should be freshly prepared before each assay.

[0299] For compounds of unknown activity or ones with MIC values of >4 ug/ml, a range of concentrations from 128 ug/ml to 0.125 ug/ml should be used. More active compounds, such as Amphotericin B (Sigma A2411) and Itraconazole (Research Diagnostics Inc. cat#30.211.44), require a lower range of concentrations (16 ug/ml to 0.016 ug/ml). Stock solutions of Amphotericin B and Itraconazole should be prepared at 1.6 mg/ml in DMSO. Amphotericin B is sold as a powder that is approximately 80% Amphotericin B. Stock solutions should be made accordingly (2.0 mg of powder for a 1 ml solution of 1.6 mg/ml Amphotericin B).

[0300] Stock solutions of control compounds (1.6 mg/ml, Amphotericin B or Itraconazole) are initially diluted in medium to a concentration of 32 ug/ml while stock solutions of test compounds (typically 12.8 mg/ml) are diluted to 256 ug/ml. Both of these (control and test compounds) represent 1:50 dilutions. For an assay with three fungal strains, 40 microliters of a stock solution should be diluted to 2.0 ml with room temperature medium. If a stock solution of a test compound is not at 12.8 mg/ml, the appropriate dilution must be calculated. Serial dilutions will be produced (see below) using these initial dilutions. Addition of cells to compound will produce an additional two-fold dilution.

[0301] Natural product extracts are tested at concentrations ranging from 200 to 204,800 fold dilution of the extract based upon the initial culture volume. The extract should first be diluted 100 fold then serial dilutions produced as directed below.

Assay Setup

[0302] Antifungal susceptibility tests should be setup in polystyrene, 96-well, flat bottom plates (Costar 9017). To every well in columns 2-12 is added 100 microliters of media. An electronic multichannel (12) pipettor with no tip on channel one makes this job simple. To every well in column one is added 200 microliters of diluted compound (32 ug/ml for Amphotericin B and Itraconazole controls, 256 ug/ml for test compounds, 100-fold dilution for natural product extracts). A manual multichannel (8) pipettor is then used to set up a series of 2-fold dilutions. 100 microliters is removed from each well of column one and mixed with 100 microliters in column 2. This is done successively (column two to column three etc.) to produce a set of 11 serial dilutions (column 12 is a drug free control).

[0303] To every well in two rows, 100 ul of inoculum (2×) of a single strain is added. To the final two rows on the plate (G & H), only media is added. Addition of inoculum is best accomplished using an electronic multichannel (12) pipettor. This setup (see below) creates a starting cell density of 500-2500 per ml (100-500 per well) and drug concentration ranging from 16 ug/ml to 0.016 ug/ml for controls (Amphotericin B and Itraconazole), 128 ug/ml to 0.125 ug/ml for pure test compounds, and 200 to 204,800-fold dilutions for natural product extracts.

[0304] It is important to determine the number of colony forming units (CFUs) present in each strain inoculum (2×). Two 100 ul aliquots of each inoculum (2×) should be spread on SDA plates and incubated at 35° C. for 1-2 days to determine the precise number of colony forming units. An acceptable range for the inoculum (2×) is 1-5×10³ cfu/ml (100-500 for 100 ul). Following two-fold dilution of the inoculum with compound, the final concentration of cells will be 0.5-2.5×10³ per ml. The plates should then be placed in a dark, 35° C. incubator for 48 hours.

Modified Assay Setup for Low Solubility Compounds

[0305] Some compounds are not very soluble in aqueous media even at low concentrations and dilution artifacts can result from precipitation of the compounds. To avoid such problems a series of two fold dilutions at 100 times the final concentration is prepared from the stock solution in the same solvent (typically DMSO). Each intermediate solution is then diluted to final strength with 1× inoculum.

[0306] This type of assay setup involves making a series of 11, 2-fold dilutions in DMSO ranging from 12,800 ug/ml to 12.5 ug/ml for test compounds and 1600 ug/ml to 1.6 ug/ml for control compounds (Amphotericin B and itraconazole). Two microliters of diluted compound are placed into each well of the appropriate column (12,800 ug/ml in column 1, down to 12.5 ug/ml in column 11, and DMSO to column 12). To every well in two rows, 200 ul of inoculum (1×) of a single strain is added. To the final two rows on the plate (G & H), only media (200 ul) is added. Addition of inoculum is best accomplished using an electronic multichannel (12) pipettor. Final concentrations of cells and compounds are the same as described above for the standard assay setup. Please note that the inoculum in this assay is at 1× concentration, while the inoculum for the assay described above is a 2× concentrate. The 1× inoculum is made by adding an equal volume of media to the 2× inoculum.

[0307] NCCLS recommends using this type of assay setup for insoluble compounds, including Amphotericin B and Itraconazole. While we are able to obtain reasonably consistent results for Amphotericin B and Itraconazole using the standard assay setup, some test compounds may benefit from doing the serial dilutions in DMSO. Compounds that form heavy precipitates upon dilution to media should be considered for this assay, particularly if the compound seems to be a promising candidate or inconsistent results are obtained in the standard assay.

Reading the Results

[0308] Minimum Inhibitory Concentration (MIC): The MIC is the lowest concentration of an antifungal agent that inhibits growth of the organism. For Amphotericin B, the lowest drug concentration which gives no visible growth is the MIC. For Itraconazole (and other azoles), the lowest drug concentration which reduces growth to ≦20% of the growth control (column 12) is the MIC.

[0309] For test compounds that give a sharp endpoint (like Amphotericin B), the lowest drug concentration which gives no visible growth is the MIC. For test compounds that give a trailing effect on inhibition of cell growth (like the azoles), the lowest drug concentration which reduces growth to ≦20% of the growth control (as determined by measurement of turbidity) is the MIC.

[0310] The turbidity of each well is determined by measuring the absorbance at 415 nm on a plate reader (BIO-RAD Model 3550-UV). The rows containing no cells (G & H) serve as a control for absorbance. Column 12, containing no compound, serves as the growth control.

[0311] Minimum Fungicidal Concentration (MFC): The MFC is the lowest concentration of an antifungal agent that results in an inviable culture. Two slightly different standards and assays are applied, depending on the circumstances. For each of the two methods, though, culture viability should be determined beginning with the drug dilution immediately below the MIC and continuing through to the highest drug concentration.

[0312] The first and more rigorous standard considers a culture to be inviable if it contains ≦1% of the colony forming units of the starting culture. This is determined by completely removing the cells from a well of the microtiter plate and placing them in a microfuge tube containing 1.3 ml of RPMI media. The cells are spun for 2 minutes, supernatant poured off, cells resuspended in the remaining media, and spread on an SDA plate. The plate is incubated at 35° C. for 1-2 days, and the colonies counted. These numbers are compared to the original cfu count from day 1 of the assay.

[0313] A second, simpler method is more practical for processing a large number of samples and is the method that we routinely use. Following resuspension of the cells by pipetting, 15 microliters is spotted directly to an SDA plate and incubated for 2 days at 35° C. A culture is considered inviable if no colonies form on the plate. While this method is much simpler than the one above, it is less quantitative and no efforts are made to wash the compound away from the cells before plating. One may observe inhibition of growth on the agar plate if a compound is still present at high enough concentrations

[0314] The control compound Amphotericin B is a cidal drug and the MIC is typically equal to the MFC. Itraconazole, in contrast, is a static drug and viable cells should be recovered from wells containing compound at concentrations well above the MIC.

Quality Control

[0315] Cell density of the inoculum (2×) must be between 1 and 5×10³ cfu/ml (100-500 cfu per 100 microliters). Starting cell concentration in the assay will be 0.5 to 2.5×10³ cfu/ml. Acceptable MIC range values (ug/ml): Am B Itraconazole Candida albicans, e.g., ATCC 10231 0.25-1.0 0.25-1.0 Saccharomyces cerevisiae, e.g., CTY552 0.25-1.0 0.25-1.0 Aspergillus nidulans, e.g., NRRL 194 (ATCC 38163) 0.5-2.0 0.25-1.0

[0316] If the starting cell density or MIC values do not fall within the acceptable range, all results in the assay for the particular strain in question are considered invalid and the assay should be repeated.

Secondary Screens—Mechanistic Assays

[0317] The preferred inhibitor compounds of the invention are those which possess antifungal activity, although compounds with significant activity in an in vitro mechanism-based assay may be considered for further development. Such secondary assays are performed to determine the mechanism of action of these compounds. Such secondary mechanistic assays include in vitro experiments, as well as and in vivo experiments in fungi, to determine the mechanistic inhibitory activity of these compounds. The precise nature of these assays will depend on the target.

[0318] Compounds that prevent cell growth through inhibition of the target protein are considered for further development.

Counterscreening in Other Species

[0319] In parallel to secondary screen assays, counterscreens are performed to determine if the compounds inhibit the activity of any human homolog. The precise nature of the counterscreen(s) will depend on the nature of the target protein. These counterscreens may include an affinity assay to determine if the compound binds the human homolog or an in vitro or cell-based mechanistic assay to determine if the compound inhibits the activity of the human protein.

[0320] Cytotoxicity studies on mammalian cells are also performed to determine if the compound is toxic to mammalian cells in culture. Compounds that do not bind to and/or inhibit the activity of the human homolog will be considered for further development.

Transcription Inhibition Counterscreen Using Human Homolog

[0321] When the essential target protein has been identified as being required for growth and as an inhibitor of Candida albicans according to one or more of the assays described herein, it may be tested further in order to determine its effect on the host organism. In the development of useful antifungal compounds for human therapeutics, it is desirable that such compounds act as effective agents in inhibiting the viability of the fungal pathogen while not significantly inhibiting human cell systems. Specifically, inhibitors of Candida albicans identified in any one of the above described assays may be counterscreened for inhibition of a human homolog of the target protein.

[0322] If available, the human gene encoding for the target protein can be expressed and purified utilizing published methods and its homology to the yeast target protein homolog(s). The human homolog can be contacted with candidate inhibitor in assays such as those described above using a human cell culture system. The effectiveness of a C. albicans inhibitor as a human therapeutic is determined as one which exhibits a low level of inhibition against its human homolog relative to the level of inhibition with respect to the C. albicans target protein. For example, it is preferred that the amount of inhibition by a given inhibitor of the human homolog in a human system be no more than 20% with respect to the amount of inhibition of the C. albicans target protein.

[0323] Such inhibitors are “selective inhibitors” of the C. albicans target protein which “selectively inhibit” C. albicans biological activity. The lack of effect of a test compound on mammalian transcription or other growth-related mechanisms is tested by replacing yeast components with an analogous human in vitro transcription system as in e.g. Manley et al. Proc.Natl.Acad.Sci. USA 77:3855, 1980.

[0324] An example of one such mammalian cytotoxicity screening method is described in Example 3.

Chemical Analoging

[0325] It is important to note that some compounds may prove to be cytotoxic, but not inhibitory of the activity of the human homolog. Compounds that exhibit such non-target based cytotoxicity are still considered for further development. Chemical analoging efforts may be used to separate the target-based antifungal activity from the non-target-based cytotoxicity activity.

[0326] Chemical analoging is also used to identify compounds with improved antifungal activity and reduced cytotoxicity. The secondary assays and counterscreens described above are used in parallel with antifungal assays to ensure that compounds remain active against the appropriate target, i.e., remain inhibitory with the same mechanism of action.

[0327] Antifungal testing against a broad spectrum of fungal species and a large number of isolates is also performed at this point. The broad spectrum of fungal species will include those resistant to existing therapeutics, e.g., Amphotericin B and various azoles such as, for example, intraconzole and fluconazole. Compounds which inhibit growth of fungi, particularly Candida and Aspergillus species, at a concentration of 4 ug/ml or less, exhibit minimal cytotoxicity, and have a confirmed mechanism of action are considered for further development..

Preclinical Development of Candidate Drugs

[0328] Subsequent preclinical development of compounds includes, but is not limited to: formulation, toxicology, pharmacokinetics, animal efficacy studies, and medicinal chemistry. Compounds with the desired characteristics are selected for clinical trials in human subjects.

Dosage and Pharmaceutical Formulations

[0329] For therapeutic uses, inhibitors identified as described herein may be administered in a pharmaceutically acceptable/biologically compatible formulation. The compositions of the present invention can be administered in dosages and by techniques well known to those skilled in the medical, veterinary, and agricultural arts taking into consideration such factors as the age, sex, weight, species and condition of the particular patient, and the route of administration. The compositions of the present invention can be administered alone or in combination, or can be co-administered or sequentially administered with additional antifungal agents, such as, e.g., nystatin, amphotericin B, flucytosine and the various antifungal azoles.

[0330] Such pharmaceutical compositions can be used in particular for treatment of topical and systemic fungal infections and can be administered bucally, rectally, parenterally or locally by topical application to the skin and the mucous membranes, or by intravenous or intramuscular injection. These compositions can be solid or liquid and can be in any of the pharmaceutical forms generally used in human medicine, such as, for example, simple or coated tablets, capsules, granules, suppositories, injectable preparations, ointments, creams, gels and aerosol preparations. The pharmaceutical compositions of the invention are prepared by the usual methods known to those of ordinary skill in the art. The active principle can be incorporated in them with excipients usually employed in pharmaceutical compositions, such as talc, gum arabic, lactose, starch, magnesium stearate, cacao butter, aqueous or non-aqueous vehicles, fatty substances of animal or plant origin, paraffin derivatives, glycols, various wetting, dispersing or emulsifying agents and preservatives.

[0331] Liquid preparations are useful for 1) mucosal administration, e.g., oral, nasal, anal, vaginal, peroral, intragastric administration and the like, in the form of solutions, suspensions, syrups, elixirs; and 2) topical administration e.g., in the form of a cream, ointment, lotion or spray. Further, liquid pharmaceutical formulations comprising the inhibitors to be used for parenteral, subcutaneous, intradermal, intramuscular, intravenous administrations, and the like, such as sterile solutions, suspensions or emulsions, e.g, for administration by injection, can be formulated without undue experimentation.

[0332] In order for a composition to be administered to an animal or human, and for any particular method of administration, it is preferred to determine the toxicity, such as by determining the lethal dose (LD) and LD₅₀ in a suitable animal model, e.g., mouse; the dosage of the composition(s), and the concentration of components in the composition; and the timing of administration in order to maximize the antiviral and/or antimicrobial response. Such factors can be determined without undue experimentation by such methods as titrations and analysis of sera for antibodies or antigens, e.g., by ELISA and/or EFFIT analysis. Such determinations do not require undue experimentation from the knowledge of the skilled artisan, the present disclosure and the documents cited herein.

[0333] The formulations can be administered in a pharmaceutically effective amount and/or an antifungal effective amount, taking into account such factors as the relative activity and toxicity for the target indication, e.g., antifungal activity, as well as the route of administration, and the age, sex, weight, species and condition of the particular patient.

[0334] As discussed above, the pharmaceutical compositions of the present invention can be solutions, suspensions, emulsions, syrups, elixirs, capsules, tablets, creams, lotions and the like. The compositions may contain a suitable carrier, diluent, or excipient, such as sterile water, physiological saline, glucose, or the like. Moreover, the compositions can also be lyophilized, and/or may contain auxiliary substances, such as wetting or emulsifying agents, pH buffering agents, adjuvants, gelling or viscosity enhancing additives, preservatives, flavoring agents, colors, and the like, depending upon the route of administration and the preparation desired. Standard texts, such as “Remington's Pharmaceutical Science”, 17th Ed., 1985, incorporated herein by reference, may be consulted to prepare suitable preparations, without undue experimentation.

[0335] The amount of inhibitor administered will be determined according to the degree of pathogenic infection and whether the infection is systemic or localized, and will typically be in the range of about 1 ug-100 mg/kg body weight. Where the inhibitor is a peptide or polypeptide, it will be administered in the range of about 100-500 ug/mL per dose. A single dose of inhibitor or multiple doses, daily, weekly, or intermittently, is contemplated according to the invention.

[0336] The route of administration will be chosen by the physician, and may be topical, oral, transdermal, nasal, rectal, intravenous, intramuscular, or subcutaneous.

[0337] The following examples are intended as non-limiting illustration of the present invention.

EXAMPLE 1 S. cerevisiae Inactivation Analysis Yeast Genomic DNA Preparation

[0338] This protocol can be used to prepare genomic DNA from Candida albicans cultures as well as Saccharomyces cerevisiae. Streak a yeast stock culture from a glycerol stock to a YPD (Bio101 Cat# 4001-242) plate and incubated for 48 hours at 30° C. Pick a single, distinct colony into 5 ml of YPD media (Bio100 Cat# 4001-042), and incubate overnight at 30° C. in a roller drum. Cells from 1 ml of this culture are pelleted with a 5 second spin in a microcentrifuge. The cells are washed one time with 1 ml TE (10 mM Tris-Cl, pH 8.0, 1 mM EDTA) and respun. Resuspend the pellet in 0.2 ml Extraction Buffer (2% TritonX100, 1% SDS, 100 mM NaCl, 10 mM Tris pH 7.5 and 1 mM EDTA) and add 0.2 ml phenol/chloroform/isoamyl (25:24:1, v:v:v). Add 0.3 g acid washed 400 micron glass beads. Vortex for 5 minutes. Add 0.2 ml TE; spin in a microcentrifuge for 10 minutes at 10-13 krpm. Remove the aqueous phase to a fresh tube. Precipitate with 2.5 volumes absolute ethanol. Spin and resuspend the pellet in 400 ul TE plus 3 ul of a 10 mg/ml RNase A stock. Incubate at 37° C. for 5 minutes. Add 10 ul 4 M ammonium acetate and 1 ml absolute ethanol. Mix by inversion and centrifuge for 8 minutes in a microcentrifuge. Air dry the pellet and resuspend in 50 ul TE. Store at 40° C. The solution may appear somewhat cloudy. Before diluting this stock for use in PCR reactions or Southern blotting, vortex the stock sample briefly.

[0339] Alternately, the YeaStar Genomic DNA Kit is available from Zymo Research (Cat. # D2002). It has the advantage of avoiding the use of glass beads and phenol:choloroform mixtures, and produces very clean genomic DNA, although in some cases it has proven to be a somewhat less reproducible method than that detailed above.

Transformation of S. cerevisiae

[0340] Streak strain to a rich media plate (such as YPD) and incubate at 30° C. for 48 hours. Pick a single distinct colony to 2-5 ml YPD media and incubate overnight on a roller drum. Dilute to A600=0.2 in 200 ml YPD and incubate at 30° C. until A₆₀₀=0.8 (about 4 hours growth under normal circumstances). Divide the culture into 4 sterile 50 ml tubes. Centrifuge at medium low speed, for instance in a Beckman JT-6 at 3000 rpm for 5 minutes. Resuspend and combine the pellets in 20 ml H₂O. Re-centrifuge. Resuspend the pellet in 10 ml TEL (10 mM Tris pH 7.5, 1 mM EDTA, 0.1 M lithium acetate). Recentrifuge again and resuspend in 2 ml TEL. Competent cells are stable at room temperature for up to four hours. If you wish to make frozen stocks, you may add sterile glycerol (from a 50% stock) to a final concentration of 15%, then freeze by placing in a −80° C. freezer (do not quick freeze in liquid nitrogen or dry ice/ethanol bath). The frozen competent cells can be expected to be 3-5 fold less competent than freshly made competent cells.

[0341] Add 100 μg well sheared single stranded carrier DNA and the 30 μl digested plasmid DNA to a clean eppendorf tube. Add 100 ml competent cells and mix. Add 0.8 ml PLATE (40% PEG-3350 10 mMTris pH7.5, 1 mM EDTA, 0.1 M lithium acetate) and mix well. Incubate 30 minutes at 30° C. Heat shock 20 minutes at 42° C. Centrifuge for 5 seconds in a microcentrifuge and remove the supernatant. Wash the pellet with 1 ml TE, spin again and plate the pellet in a minimal volume (<50 μl) onto selective media such as (−)HIS plates.

[0342] TEL and PLATE solutions are available commercially (SIGMA Cat. T-0809 and P-8966), and seem to be stable at room temperature. We have found that for TEL and PLATE made in the laboratory, the solutions work best if made fresh the day of the transformation from stock solutions of Tris-Cl, EDTA, PEG-3350 and lithium acetate.

[0343] After 48 to 72 hours incubation at 30° C., depending on the growth rate of the specific strain, individual colonies are coordinately struck with a sterile toothpick to two identically arrayed plates, one of which is (−)HIS and one of which is (−)HIS (+)Cu. Pick at least 12 colonies in this manner and incubate the resultant plates for 48-72 hours (again, depending on the strain growth rate) at 30° C. Be sure to pick a colony or two of CUY106 as a positive control for growth on the (−) HIS (+) Cu plate. After incubation, the plates are scored for growth. In the case of true copper sensitive strains, there will be a clear lack of growth on the (−) HIS (+) Cu plates, and clear growth on the (−)HIS plates.

Copper Titration

[0344] Single colonies from a selective plate (see above) are picked to CSM media (Bio101 Cat. # 4500-022) and grown overnight at 30° C. in a roller drum. The use of Bio101 CSM appears to be critical to the reproducibility of the titrations. Cultures are diluted to A600 =0.2 and are 2 ml portions are aliquoted to sterile capped culture tubes. From a 500 mM stock, copper sulfate is added to each tube to final concentrations of 0 uM ((−) copper control), 10 uM, 20 uM, 50 uM, 100 uM, 200 uM, 500 uM 1.0 mM, 1.5 mM and 2.0 mM. The ten tubes are incubated at 30° C. on a roller drum for 16-20 hours. The A600 of each aliquot is measured, and the results are graphed on a semi-log plot: Y axis=A600 of sample normalized to the A600 of the (−)copper control (linear scale). X axis=concentration of CuSO₄ (log scale).

Copper Time Course

[0345] Single colonies from a selective plate (see above) are picked to CSM media (Bio101 Cat. # 4500-022) and grown overnight at 30° C. in a roller drum. As is the case for the copper titrations, the use of Bio101 CSM appears to be critical to the reproducibility of the copper time courses. Cultures are diluted in 25 ml of CSM to A600=0.02-0.1. the cultures are split evenly between two sterile 50 ml tubes and allowed to grow in a shaker/incubator for 1 hour at 30° C. Addition of 1 mM copper sulfate (from a 500 mM sterile stock) to one of the cultures defines the 0 time point. At each time point, a 1.2 ml aliquot is taken from each culture for analysis, and the cultures are quickly returned to incubation at 30° C. with shaking. The exception to this is the 0 time point, at which time only the culture which does not receive added copper is assayed as the data point for both the cultures. Part of each aliquot is used to measure the A600, while the rest is used to perform a serial 10-fold dilution series: 100 ul of the aliquot is diluted serially with 900 ul aliquots of sterile water. Fresh pipette tips are used for each step of the dilution series, representing 101, 102, 103, 104 and 105 fold dilutions of the original culture. Appropriate dilutions are plated to YPD plates, and the plates are marked with a strain identifier, time point, whether or not they contain copper, and which dilution has been plated. Plates are placed at 30° C. and checked both 48 and 72 hours after they have been plated; visible colonies are counted and normalized to colonies per ml of original culture, based on the dilution factor, and the plating factor (since only 100 ul and not 1 ml was plated).

[0346] Appropriate dilutions to plate to YPD:

[0347] For CUY106, and other copper insensitive strains:

[0348] At 0 time point: 10³, 10⁴, 10⁵

[0349] At time points less than 10 hours: 10³, 10⁴, 10⁵

[0350] At time points greater than 10 hours: 10⁴, 10⁵, 10⁶

[0351] For genes of unknown cidality:

[0352] At 0 time point: 10³, 10⁴, 10⁵

[0353] At time points less than 10 hours: 10¹, 10³, 10⁵

[0354] At time points greater than 10 hours: 10⁰, 10², 10⁴, 10⁶

[0355] The 100 dilution o refers to a plating of 100 μl of undiluted culture. It is recommended for cultures containing copper sulfate that the undiluted samples be spun in a microcentrifuge for 5 seconds and the pellets resuspended in sterile water before plating to YPD in order to avoid contamination by copper sulfate. For all other samples in the dilution series, this extra step has proven unnecessary. In cases of extreme cell non-survival, a second time course is recommended, to confirm the results of the first. In this case, the appropriate dilutions to plate will depend on the results of the original experiment: static effects may be more carefully assayed by biasing towards greater dilutions, while large fungicidal effects can be captured with lesser dilutions at the later time points. In some cases, we have found that concentration of the culture is necessary (for instance, concentration of 1 ml to a volume of 100 μl or even 10 ml to 100 μl to obtain a measurable number of live cells following exposure to copper (the latter case requires adjustments to the volumes used in the experiment to accommodate the large volumes needed).

[0356] Results from S. cerevisiae inactivation analyses for the target genes described in Table 1 are shown in FIGS. 27-53.

EXAMPLE 2 C. albicans Transformation

[0357] From a single colony on a plate, grow up a 1 ml overnight culture of Candida albicans in YPD supplemented with 20 μg/ml uridine. at 30° C. with agitation. Dilute the culture into 50 ml uridine-supplemented YPD and grow at 30° C. with agitation. When the A₅₄₀ of the culture reaches 2, cool the cells on ice for 10 minutes, then Centrifuge at 5000 rpm for 10 minutes at 4° C. Wash the pellet two times with 10 ml TE and recentrifuge each time. Resuspend the pellet in 1 ml TELD (10 mM Tris-Cl, 1 mM EDTA, pH 7.5, 0.01 M lithium acetate, 0.01 M DTT). It is important to make TELD fresh from 10× stocks of each of the components (10× DTT should be stored frozen). Spin briefly in a microcentrifuge. Resuspend the pellet in 200 ul TELD. This is sufficient competent yeast for 4 transformations. To a fresh tube add: 50 μl competent yeast preparation, 5 μl 10 mg/ml carrier DNA (Clontech) , 1-2 μl of digested and gel purified plasmid fragment (at 1-2 μg/ml), 300 μl of PEG Solution TELD (10 mM Tris-Cl, 1 mM EDTA, pH 7.5, 0.01 M lithium acetate, 0.01 M DTT, 40% PEG4000 (VWR Cat. # 9727-2)). Mix by inversion. Incubate 30 min at 30° C., then heat shock 20 minutes at 42° C. Spin 15 seconds in a microcentrifuge. Resuspend the pellet in 200 μl TE and spread on (−)URA plates.

EXAMPLE 3 Mammalian Cell Cytotoxicity Screen Reagents

[0358] From ATCC: CV-1 fibroblast cell line originated from a male African monkey kidney. Cat. No.: CCL-70

[0359] From Gibco BRL:

[0360] Dulbecco's modifed Eagle's Medium (“DMEM”) 1× liquid. Cat. No.: 11965-065

[0361] Dulbecco's modifed Eagle's Medium without Phenol red. Cat. No.:11054-020

[0362] Fetal bovine serum Cat. No.: 26140-079

[0363] Gentamicin reagent solution Cat. No.:15710-015

[0364] Trypsin-EDTA Cat. No.: 25300-54

[0365] From Sigma:

[0366] In vitro toxicology assay kit, XTT based. Cat. No.:TOX-21.

[0367] (XTT is 2,3-bis(2-Methoxy-4-nitro-5-sulfophenoyl)-2H-tetrazolium-5-carboxyarilideinn salt)

Procedure

[0368] 1. Split CV-1 cell at 1:20 using DMEM medium supplemented with 10% FBS and 10 g/ml gentamycin.

[0369] 2. Three days after the splitting, CV-1 cell should reach about 80-90% confluency.

[0370] 3. Aspirate the medium out and add 5 ml of PBS.

[0371] 4. Add 3 ml of trypsin and let stand for 3 minutes. Add 2 ml of DMEM to inactivate the trypsin.

[0372] 5. Take 0.5 ml of cell and diluted with 10 ml of DMEM. This should make the cell concentration in the range 0.5-1.5×10⁵ cells/ml.

[0373] 6. Add 100 μl cell suspension to row 2-8 of 96 well plates. Add medium only to row 1.

[0374] 7. Incubate cells for 24 hours.

[0375] 8. Make1:50 dilution of the compound to be tested with concentration of 12.8 mg/ml.

[0376] 9. Add 300 ul to column 1 from row 4 to row 8.

[0377] 10. Row 1 and row 2 of column 1 should be filled with 300 μl medium only. Row 3 of column 1 should be filled with 300 μl medium with 2% DMSO so that final concentration of DMSO will start with 1%.

[0378] 11. Fill columns 2 ,3, 4, 5 and 6 with 200 μl DMEM medium.

[0379] 12. Make a 1 to 3 serial dilution from column 1 to column 6.

[0380] 13. Take out 100 μl of each different conc of compound into the cell plate from column 1 to 6 and duplicate with 7-12.

[0381] 14. Incubate the cells for another 24 hours.

[0382] 15. Dissolve 5 mg of XTT into 25 ml of DMEM medium without phenol red.

[0383] 16. Take out the compound solution by aspiration.

[0384] 17. Wash the 96 well plate with 300 μl PBS and sit for 3 minutes.

[0385] 18. Add 100 μl XTT solution to column 1-6 and add DMEM medium (without phenol red) to column 7-12.

[0386] 19. Measure O.D.⁴⁵⁰ and subtract O.D.⁶⁵⁰ at the plate reader. Also, take time points at 1 hr intervals for 4 hours.

[0387] b 20. Split the CV-1 cells 1:20 using DMEM medium supplemented with 10% FBS and 10% genamycin.

[0388] XTT is a measure of mitochondrial activity and, therefore, is considered a reasonable measure of cell growth and viability. After subtracting the OD690 from OD 450, each compound-treated datapoint shall be compared with that of no-compound treatment and this determines the percentage of growth. The percentage of inhibition is defined as one minus the percentage of growth. Percentage of inhibition is plotted vs compound concentration. TC₅₀ is defined as the compound concentration that inhibits cell growth by 50%. The data from the cytotoxicity assay together with the results of the antifungal assays can be used to calculate a therapeutic ratio (TC₅₀/MIC). The higher this ratio, the more attractive the compound. Analoging and medicinal chemistry can be used to improve this ratio.

[0389] All of the references identified hereinabove, are hereby expressly incorporated herein by reference to the extent that they describe, set forth, provide a basis for or enable compositions and/or methods which may be important to the practice of one or more embodiments of the present inventions.

0 SEQUENCE LISTING <160> NUMBER OF SEQ ID NOS: 146 <210> SEQ ID NO 1 <211> LENGTH: 316 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 74 <400> SEQUENCE: 1 Met Gly Glu Val Lys Val Lys Val Gln Pro Pro Asp Ala Asp Pro Val 1 5 10 15 Glu Ile Glu Asn Arg Ile Ile Glu Leu Cys His Gln Phe Pro His Gly 20 25 30 Ile Thr Asp Gln Val Ile Gln Asn Glu Met Pro His Ile Glu Ala Gln 35 40 45 Gln Arg Ala Val Ala Ile Asn Arg Leu Leu Ser Met Gly Gln Leu Asp 50 55 60 Leu Leu Arg Ser Asn Thr Gly Leu Leu Tyr Arg Ile Lys Asp Ser Gln 65 70 75 80 Asn Ala Gly Lys Met Lys Gly Ser Asp Asn Gln Glu Lys Leu Val Tyr 85 90 95 Gln Ile Ile Glu Asp Ala Gly Asn Lys Gly Ile Trp Ser Arg Asp Ile 100 105 110 Arg Tyr Lys Ser Asn Leu Pro Leu Thr Glu Ile Asn Lys Ile Leu Lys 115 120 125 Asn Leu Glu Ser Lys Lys Leu Ile Lys Ala Val Lys Ser Val Ala Ala 130 135 140 Ser Lys Lys Lys Val Tyr Met Leu Tyr Asn Leu Gln Pro Asp Arg Ser 145 150 155 160 Val Thr Gly Gly Ala Trp Tyr Ser Asp Gln Asp Phe Glu Ser Glu Phe 165 170 175 Val Glu Val Leu Asn Gln Gln Cys Phe Lys Phe Leu Gln Ser Lys Ala 180 185 190 Glu Thr Ala Arg Glu Ser Lys Gln Asn Pro Met Ile Gln Arg Asn Ser 195 200 205 Ser Phe Ala Ser Ser His Glu Val Trp Lys Tyr Ile Cys Glu Leu Gly 210 215 220 Ile Ser Lys Val Glu Leu Ser Met Glu Asp Ile Glu Thr Ile Leu Asn 225 230 235 240 Thr Leu Ile Tyr Asp Gly Lys Val Glu Met Thr Ile Ile Ala Ala Lys 245 250 255 Glu Gly Thr Val Gly Ser Val Asp Gly His Met Lys Leu Tyr Arg Ala 260 265 270 Val Asn Pro Ile Ile Pro Pro Thr Gly Leu Val Arg Ala Pro Cys Gly 275 280 285 Leu Cys Pro Val Phe Asp Asp Cys His Glu Gly Gly Glu Ile Ser Pro 290 295 300 Ser Asn Cys Ile Tyr Met Thr Glu Trp Leu Glu Phe 305 310 315 <210> SEQ ID NO 2 <211> LENGTH: 330 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 75 <400> SEQUENCE: 2 Met Ser Glu Met Leu Val Ser Asp Lys Ala Arg His Leu Tyr Thr Lys 1 5 10 15 Met Arg Glu Tyr Pro Thr Ser Lys Leu Phe Asp Gln Asp Glu Leu Gln 20 25 30 Thr Leu Phe Asp Ile Lys Lys Gly Ser Glu Leu Met Glu Tyr Leu Gln 35 40 45 Glu Leu Val Asn Gly Lys Tyr Val Lys Ile Ser Lys Met Gly Asp Gln 50 55 60 Leu Lys Phe Gln Thr Val Ala Glu Glu Glu Ala Lys Lys Val Ser Ser 65 70 75 80 Met Ser Asp Asp Glu Ala Met Ile Tyr Ser Tyr Ile Glu Ala Ser Gly 85 90 95 Arg Glu Gly Ile Trp Thr Lys Thr Ile Lys Ala Lys Thr Asn Leu His 100 105 110 Gln His Ile Val Gln Lys Cys Leu Lys Asn Leu Glu Asn Asn Arg Tyr 115 120 125 Ile Lys Ser Ile Lys Ser Val Lys His Pro Thr Arg Lys Ile Tyr Met 130 135 140 Leu Tyr Asn Leu Gln Pro Ser Ile Asp Val Thr Gly Gly Pro Trp Phe 145 150 155 160 Thr Asp Ser Glu Leu Asp Thr Glu Phe Ile Glu Thr Leu Leu Glu Val 165 170 175 Cys Trp Arg Phe Ile Val Gly Lys Thr Met Tyr Ile Lys Asp Glu Glu 180 185 190 Ala Asp Asn Glu Asp Ile Asn Pro Leu Gln Thr Thr Tyr His Asn His 195 200 205 His Pro Gly Val Asn Leu Asp Gln Leu Val Glu Phe Ile Asn Asn Ser 210 215 220 Asn Ile Thr Ser Val Glu Leu Gly Ile Asn Asp Ile Arg Ser Leu Cys 225 230 235 240 Asp Val Leu Ile Tyr Asp Asp Arg Ile Glu Glu Val Gly Gly Asn Gln 245 250 255 Glu Asn Ser Gly Ile Phe Lys Ala Thr Trp Gln Ser Ile Ile Asp Lys 260 265 270 Gly Asn Thr Ile Leu Gln Asn Asn Tyr Gln Asp Leu Lys Asn Val Val 275 280 285 Ser Glu Asp Cys Phe Asn Tyr Leu Gln Gln Asn Gln Ser Asp Phe Ser 290 295 300 Val Phe Gln Tyr Lys Ser Thr Ile Gln Asp Leu Gln Asp Glu Ser Asp 305 310 315 320 Leu Val Tyr Leu Asp Ser Trp Met Asn Glu 325 330 <210> SEQ ID NO 3 <211> LENGTH: 317 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/U93869 <309> DATABASE ENTRY DATE: 1997-06-23 <313> RELEVANT RESIDUES: (1)..(317) <400> SEQUENCE: 3 Met Ser Gly Met Ile Glu Asn Gly Leu Gln Leu Ser Asp Asn Ala Lys 1 5 10 15 Thr Leu His Ser Gln Met Met Ser Lys Gly Ile Gly Ala Leu Phe Thr 20 25 30 Gln Gln Glu Leu Gln Lys Gln Met Gly Ile Gly Ser Leu Thr Asp Leu 35 40 45 Met Ser Ile Val Gln Glu Leu Leu Asp Lys Asn Leu Ile Lys Leu Val 50 55 60 Lys Gln Asn Asp Glu Leu Lys Phe Gln Gly Val Leu Glu Ser Glu Ala 65 70 75 80 Gln Lys Lys Ala Thr Met Ser Ala Glu Glu Ala Leu Val Tyr Ser Tyr 85 90 95 Ile Glu Ala Ser Gly Arg Glu Gly Ile Trp Ser Lys Thr Ile Lys Ala 100 105 110 Arg Thr Asn Leu His Gln His Val Val Leu Lys Cys Leu Lys Ser Leu 115 120 125 Glu Ser Gln Arg Tyr Val Lys Ser Val Lys Ser Val Lys Phe Pro Thr 130 135 140 Arg Lys Ile Tyr Met Leu Tyr Ser Leu Gln Pro Ser Val Asp Ile Thr 145 150 155 160 Gly Gly Pro Trp Phe Thr Asp Gly Glu Leu Asp Ile Glu Phe Ile Asn 165 170 175 Ser Leu Leu Thr Ile Val Trp Arg Phe Ile Ser Glu Asn Thr Phe Pro 180 185 190 Asn Gly Phe Lys Asn Phe Glu Asn Gly Pro Lys Lys Asn Val Phe Tyr 195 200 205 Ala Pro Asn Val Lys Asn Tyr Ser Thr Thr Gln Glu Ile Leu Glu Phe 210 215 220 Ile Thr Ala Ala Gln Val Ala Asn Val Glu Leu Thr Pro Ser Asn Ile 225 230 235 240 Arg Ser Leu Cys Glu Val Leu Val Tyr Asp Asp Lys Leu Glu Lys Val 245 250 255 Thr His Asp Cys Tyr Arg Val Thr Leu Glu Ser Ile Leu Gln Met Asn 260 265 270 Gln Gly Glu Gly Glu Pro Glu Ala Gly Asn Lys Ala Leu Glu Asp Glu 275 280 285 Glu Glu Phe Ser Ile Phe Asn Tyr Phe Lys Met Phe Pro Ala Ser Lys 290 295 300 His Asp Lys Glu Val Val Tyr Phe Asp Glu Trp Thr Ile 305 310 315 <210> SEQ ID NO 4 <211> LENGTH: 195 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 77 <400> SEQUENCE: 4 Met Ser Gly Ser Leu Lys Ser Leu Asp Lys Lys Ile Ala Lys Arg Arg 1 5 10 15 Gln Val Tyr Lys Pro Val Leu Asp Asn Pro Phe Thr Asn Glu Ala His 20 25 30 Met Trp Pro Arg Val His Asp Gln Pro Leu Ile Trp Gln Leu Leu Gln 35 40 45 Ser Ser Ile Ile Asn Lys Leu Ile His Ile Gln Ser Lys Glu Asn Tyr 50 55 60 Pro Trp Glu Leu Tyr Thr Asp Phe Asn Glu Ile Val Gln Tyr Leu Ser 65 70 75 80 Gly Ala His Gly Asn Ser Asp Pro Val Cys Leu Phe Val Cys Asn Lys 85 90 95 Asp Pro Asp Val Pro Leu Val Leu Leu Gln Gln Ile Pro Leu Leu Cys 100 105 110 Tyr Met Ala Pro Met Thr Val Lys Leu Val Gln Leu Pro Lys Ser Ala 115 120 125 Met Asp Thr Phe Lys Ser Val Ser Lys Tyr Gly Met Leu Leu Leu Arg 130 135 140 Cys Asp Asp Arg Val Asp Lys Lys Phe Val Ser Gln Ile Gln Lys Asn 145 150 155 160 Val Asp Leu Leu Gln Phe Pro Trp Leu Asn Ala Ile Lys Tyr Arg Pro 165 170 175 Thr Ser Val Lys Leu Leu Lys Thr Thr Val Pro Ile Val Ser Lys Lys 180 185 190 Arg Gln Lys 195 <210> SEQ ID NO 5 <211> LENGTH: 220 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 78 <400> SEQUENCE: 5 Met Asn Lys Ser Asn Lys Val Lys Lys Pro Ser Val Ala Lys Val Ser 1 5 10 15 Thr Lys Ala Ala Ser Ser Ser Leu Lys Ser Gln Glu Ala Lys Arg Gln 20 25 30 Val Phe Arg Pro Ile Leu Asp Asn Ser Phe Thr Gln Ser Asn Gln Trp 35 40 45 Pro Phe Ile Glu Pro Thr Ile Ala Asn Asp Ile Val Asp Leu Leu Glu 50 55 60 Val Leu Leu Lys Met Gln Asp Ser Thr Phe Lys Tyr Arg Gly Phe Asn 65 70 75 80 Pro Thr Val Ser Ala Leu Glu Lys Gln Ala Ala Ala Asn Arg Gly Ile 85 90 95 His Lys Asn Ala Cys Val Gln Ile Lys Tyr Val Phe Val Cys Lys Tyr 100 105 110 Asp Ile Ser Pro Ala Thr Leu Thr Asn Val Phe Pro Thr Leu Cys Phe 115 120 125 Thr Ala Ser Lys Ser Ala Glu Asp Arg Val Lys Leu Ile Gln Leu Pro 130 135 140 Arg Gly Ser Leu Glu Arg Leu Ser Lys Ala Leu Gly Val Asp Arg Val 145 150 155 160 Gly Ile Phe Gly Leu Thr Lys Asp Thr Glu Gly Ala Gln Pro Leu Phe 165 170 175 Asp Leu Ile Asn Glu Asn Val Lys Asp Ile Glu Ala Pro Trp Leu Asp 180 185 190 Cys Ile Phe Arg Glu Glu Met Val Phe Asn Gln Pro Asn Thr Lys His 195 200 205 Val Ala Ser Thr Val Gly Arg Lys Lys Asn Lys Lys 210 215 220 <210> SEQ ID NO 6 <211> LENGTH: 328 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 79 <400> SEQUENCE: 6 Met Ser Lys Asn Arg Asp Pro Leu Leu Ala Asn Leu Asn Ala Phe Lys 1 5 10 15 Ser Lys Val Lys Ser Ala Pro Val Ile Ala Pro Ala Lys Val Gly Gln 20 25 30 Lys Lys Thr Asn Asp Thr Val Ile Thr Ile Asp Gly Asn Thr Arg Lys 35 40 45 Arg Thr Ala Ser Glu Arg Ala Gln Glu Asn Thr Leu Asn Ser Ala Lys 50 55 60 Asn Pro Val Leu Val Asp Ile Lys Lys Glu Ala Gly Ser Asn Ser Ser 65 70 75 80 Asn Ala Ile Ser Leu Asp Asp Asp Asp Asp Asp Glu Asp Phe Gly Ser 85 90 95 Ser Pro Ser Lys Lys Val Arg Pro Gly Ser Ile Ala Ala Ala Ala Leu 100 105 110 Gln Ala Asn Gln Thr Asp Ile Ser Lys Ser His Asp Ser Ser Lys Leu 115 120 125 Leu Trp Ala Thr Glu Tyr Ile Gln Lys Lys Gly Lys Pro Val Leu Val 130 135 140 Asn Glu Leu Leu Asp Tyr Leu Ser Met Lys Lys Asp Asp Lys Val Ile 145 150 155 160 Glu Leu Leu Lys Lys Leu Asp Arg Ile Glu Phe Asp Pro Lys Lys Gly 165 170 175 Thr Phe Lys Tyr Leu Ser Thr Tyr Asp Val His Ser Pro Ser Glu Leu 180 185 190 Leu Lys Leu Leu Arg Ser Gln Val Thr Phe Lys Gly Ile Ser Cys Lys 195 200 205 Asp Leu Lys Asp Gly Trp Pro Gln Cys Asp Glu Thr Ile Asn Gln Leu 210 215 220 Glu Glu Asp Ser Lys Ile Leu Val Leu Arg Thr Lys Lys Asp Lys Thr 225 230 235 240 Pro Arg Tyr Val Trp Tyr Asn Ser Gly Gly Asn Leu Lys Cys Ile Asp 245 250 255 Glu Glu Phe Val Lys Met Trp Glu Asn Val Gln Leu Pro Gln Phe Ala 260 265 270 Glu Leu Pro Arg Lys Leu Gln Asp Leu Gly Leu Lys Pro Ala Ser Val 275 280 285 Asp Pro Ala Thr Ile Lys Arg Gln Thr Lys Arg Val Glu Val Lys Lys 290 295 300 Lys Arg Gln Arg Lys Gly Lys Ile Thr Asn Thr His Met Thr Gly Ile 305 310 315 320 Leu Lys Asp Tyr Ser His Arg Val 325 <210> SEQ ID NO 7 <211> LENGTH: 284 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 80 <400> SEQUENCE: 7 Met Ser Asp Leu Ser Ala Gln Leu Ser Ala Phe Lys Asn Lys Ile Lys 1 5 10 15 Ser Gly Pro Ser Val Ile Val Pro Arg Lys Ala Thr Phe Thr Gln Ser 20 25 30 Pro Ser Ser Pro Leu Ser Ser Ser Thr Thr Thr Thr Thr Ser Lys Asn 35 40 45 Asp Ala Asn Val Lys Lys Arg Ser Thr Thr Asp Ser Val Thr Arg Val 50 55 60 Leu Lys Lys Gln Lys Ala Asn Met Gly Glu Met Thr Gly Ser His Leu 65 70 75 80 Ser Thr Gln Leu His Leu Ala Val Glu Tyr Ile Lys Glu His Asp Gln 85 90 95 Pro Ile Ser Val Glu Lys Leu Gln Asn Tyr Leu Ser Phe Asp Ile Ser 100 105 110 His Thr Leu Leu Pro Leu Leu Asn Glu Ile Asp Arg Val Lys Tyr Asp 115 120 125 Glu Ser Lys Gly Thr Leu Glu Tyr Val Ser Leu His Asn Ile Arg Ser 130 135 140 Ser Asp Asp Val Leu Glu Phe Leu Arg Arg Gln Thr Thr Phe Lys Gly 145 150 155 160 Thr Ser Val Lys Glu Leu Lys Asp Gly Trp Ala Gly Cys Val Ala Ala 165 170 175 Ile Asp Glu Leu Glu Ser Gln Gly Lys Ile Leu Val Leu Arg Asn Lys 180 185 190 Lys Glu Asn Ala Pro Arg Leu Val Trp Ala Asn Asn Gly Gly Glu Leu 195 200 205 Gly Tyr Ile Asp Thr Glu Phe Lys Asp Met Trp Asp Gln Val Lys Leu 210 215 220 Pro Glu Pro Asp Val Leu Tyr Gln Lys Leu Leu Asp Gln Gly Leu Lys 225 230 235 240 Pro Thr Gly Ala Asp Pro Asn Leu Ile Lys Lys Gln Pro Gln Gln Lys 245 250 255 Glu Lys Lys Gln Lys Lys Ala Arg Arg Gly Lys Ile Thr Asn Thr His 260 265 270 Met Lys Gly Ile Leu Lys Asp Tyr Ser Gln Leu Val 275 280 <210> SEQ ID NO 8 <211> LENGTH: 291 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 81 <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/NP_002086 <309> DATABASE ENTRY DATE: 2000-10-31 <313> RELEVANT RESIDUES: (1)..(291) <400> SEQUENCE: 8 Met Asp Pro Ser Leu Leu Arg Glu Arg Glu Leu Phe Lys Lys Arg Ala 1 5 10 15 Leu Ser Thr Pro Val Val Glu Lys Arg Ser Ala Ser Ser Glu Ser Ser 20 25 30 Ser Ser Ser Ser Lys Lys Lys Lys Thr Lys Val Glu His Gly Gly Ser 35 40 45 Ser Gly Ser Lys Gln Asn Ser Asp His Ser Asn Gly Ser Phe Asn Leu 50 55 60 Lys Ala Leu Ser Gly Ser Ser Gly Tyr Lys Phe Gly Val Leu Ala Lys 65 70 75 80 Ile Val Asn Tyr Met Lys Thr Arg His Gln Arg Gly Asp Thr His Pro 85 90 95 Leu Thr Leu Asp Glu Ile Leu Asp Glu Thr Gln His Leu Asp Ile Gly 100 105 110 Leu Lys Gln Lys Gln Trp Leu Met Thr Glu Ala Leu Val Asn Asn Pro 115 120 125 Lys Ile Glu Val Ile Asp Gly Lys Tyr Ala Phe Lys Pro Lys Tyr Asn 130 135 140 Val Arg Asp Lys Lys Ala Leu Leu Arg Leu Leu Asp Gln His Asp Gln 145 150 155 160 Arg Gly Leu Gly Gly Ile Leu Leu Glu Asp Ile Glu Glu Ala Leu Pro 165 170 175 Asn Ser Gln Lys Ala Val Lys Ala Leu Gly Asp Gln Ile Leu Phe Val 180 185 190 Asn Arg Pro Asp Lys Lys Lys Ile Leu Phe Phe Asn Asp Lys Ser Cys 195 200 205 Gln Phe Ser Val Asp Glu Glu Phe Gln Lys Leu Trp Arg Ser Val Thr 210 215 220 Val Asp Ser Met Asp Glu Glu Lys Ile Glu Glu Tyr Leu Lys Arg Gln 225 230 235 240 Gly Ile Ser Ser Met Gln Glu Ser Gly Pro Lys Lys Val Ala Pro Ile 245 250 255 Gln Arg Arg Lys Lys Pro Ala Ser Gln Lys Lys Arg Arg Phe Lys Thr 260 265 270 His Asn Glu His Leu Ala Gly Val Leu Lys Asp Tyr Ser Asp Ile Thr 275 280 285 Ser Ser Lys 290 <210> SEQ ID NO 9 <211> LENGTH: 480 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 82 <400> SEQUENCE: 9 Met Ser Gln Glu Gln Tyr Thr Glu Asn Leu Lys Val Ile Val Ala Glu 1 5 10 15 Lys Leu Ala Gly Ile Pro Asn Phe Asn Glu Asp Ile Lys Tyr Val Ala 20 25 30 Glu Tyr Ile Val Leu Leu Ile Val Asn Gly Gly Thr Val Glu Ser Val 35 40 45 Val Asp Glu Leu Ala Ser Leu Phe Asp Ser Val Ser Arg Asp Thr Leu 50 55 60 Ala Asn Val Val Gln Thr Ala Phe Phe Ala Leu Glu Ala Leu Gln Gln 65 70 75 80 Gly Glu Ser Ala Glu Asn Ile Val Ser Lys Ile Arg Met Met Asn Ala 85 90 95 Gln Ser Leu Gly Gln Ser Asp Ile Ala Gln Gln Gln Gln Gln Gln Gln 100 105 110 Gln Gln Gln Gln Pro Asp Ile Ala Gln Gln Gln Pro Gln Gln Gln Pro 115 120 125 Gln Leu Gln Pro Leu Gln Pro Gln Leu Gly Thr Gln Asn Ala Met Gln 130 135 140 Thr Asp Ala Pro Ala Thr Pro Ser Pro Ile Ser Ala Phe Ser Gly Val 145 150 155 160 Val Asn Ala Ala Ala Pro Pro Gln Phe Ala Pro Val Asp Asn Ser Gln 165 170 175 Arg Phe Thr Gln Arg Gly Gly Gly Ala Val Gly Lys Asn Arg Arg Gly 180 185 190 Gly Arg Gly Gly Asn Arg Gly Gly Arg Asn Asn Asn Ser Thr Arg Phe 195 200 205 Asn Pro Leu Ala Lys Ala Leu Gly Met Ala Gly Glu Ser Asn Met Asn 210 215 220 Phe Thr Pro Thr Lys Lys Glu Gly Arg Cys Arg Leu Phe Pro His Cys 225 230 235 240 Pro Leu Gly Arg Ser Cys Pro His Ala His Pro Thr Lys Val Cys Asn 245 250 255 Glu Tyr Pro Asn Cys Pro Lys Pro Pro Gly Thr Cys Glu Phe Leu His 260 265 270 Pro Asn Glu Asp Glu Glu Leu Met Lys Glu Met Glu Arg Thr Arg Glu 275 280 285 Glu Phe Gln Lys Arg Lys Ala Asp Leu Leu Ala Ala Lys Arg Lys Pro 290 295 300 Val Gln Thr Gly Ile Val Leu Cys Lys Phe Gly Ala Leu Cys Ser Asn 305 310 315 320 Pro Ser Cys Pro Phe Gly His Pro Thr Pro Ala Asn Glu Asp Ala Lys 325 330 335 Val Ile Asp Leu Met Trp Cys Asp Lys Asn Leu Thr Cys Asp Asn Pro 340 345 350 Glu Cys Arg Lys Ala His Ser Ser Leu Ser Lys Ile Lys Glu Val Lys 355 360 365 Pro Ile Ser Gln Lys Lys Ala Ala Pro Pro Pro Val Glu Lys Ser Leu 370 375 380 Glu Gln Cys Lys Phe Gly Thr His Cys Thr Asn Lys Arg Cys Lys Tyr 385 390 395 400 Arg His Ala Arg Ser His Ile Met Cys Arg Glu Gly Ala Asn Cys Thr 405 410 415 Arg Ile Asp Cys Leu Phe Gly His Pro Ile Asn Glu Asp Cys Arg Phe 420 425 430 Gly Val Asn Cys Lys Asn Ile Tyr Cys Leu Phe Arg His Pro Pro Gly 435 440 445 Arg Val Leu Pro Glu Lys Lys Gly Ala Ala Pro Asn Ser Asn Val Pro 450 455 460 Thr Asn Glu Arg Pro Phe Ala Leu Pro Glu Asn Ala Ile Ile Glu Asn 465 470 475 480 <210> SEQ ID NO 10 <211> LENGTH: 418 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 83 <400> SEQUENCE: 10 Met Gln Phe Ala Pro Asp Asn Gln Ile Gly Lys Glu Leu Gln Gln Asn 1 5 10 15 Leu Ile Gln Glu Ile Gln Arg Arg Phe Asn Lys Pro Ala Asp Asp Ala 20 25 30 Val Asp Ile Ala Asp Tyr Ile Ile Tyr Leu Ile Val Ala Lys Lys Ser 35 40 45 Glu Gln Glu Ile Val Ala Glu Val Lys Asp Ile Ala Asp Ile Ser Ile 50 55 60 Asp Val Gly Phe Ile Gly Asp Val Tyr Leu Glu Ile Arg Lys Leu Glu 65 70 75 80 Val Lys Tyr Asn Gln Pro Pro Ala Ala Val Glu Glu Ala Ser Gln Pro 85 90 95 Gln Gln Glu Gln Gln Gln Gln Ser Gln Ala Ser Val Val Ala Pro Gln 100 105 110 Ile Pro Ile Gly Pro Lys Lys Gln Leu Thr Glu Glu Glu Lys Ile Ala 115 120 125 Leu Arg Ser Gln Arg Phe Gly Thr Thr Thr Arg Leu Ser Gly Arg Gly 130 135 140 Gly Arg Gly Gly Ile Thr Lys Thr Arg Thr Asp Phe Arg Asn Gly His 145 150 155 160 Asn Asn Lys Asn Phe Leu Asp Pro Lys Lys Leu Asp Gln Ile Ile Ser 165 170 175 Gly Ala Asn Asn Gly Ala Ile Lys Phe Val Pro Leu Pro Pro Lys Gly 180 185 190 Arg Cys Pro Asp Phe Pro Tyr Cys Lys Asn Gln Asn Cys Glu Lys Ala 195 200 205 His Pro Thr Lys Asn Cys Phe Asn Tyr Pro Asp Cys Pro Asn Pro Pro 210 215 220 Gly Thr Cys Asn Phe Leu His Pro Asp Gln Asp Gln Glu Leu Ile Ala 225 230 235 240 Lys Leu Glu Thr Ser Lys Lys Glu Phe Glu Glu Lys Lys Lys Asn Gln 245 250 255 Leu Met Val Lys Gln Gly Ser Cys Lys Tyr Gly Leu Lys Cys Ala Lys 260 265 270 Glu Asn Cys Pro Phe Ala His Pro Thr Pro Ala Asn Pro Glu Ser Gly 275 280 285 Lys Ile Glu Thr Leu Glu Trp Cys Pro Gln Gly Lys Asn Cys Gln Asp 290 295 300 Arg Asn Cys Thr Lys Ser His Pro Pro Pro Pro Thr Ala Asn Ser Glu 305 310 315 320 Lys Leu Leu Ser Ala Ala Asp Leu Ala Leu Glu Gln Cys Lys Phe Gly 325 330 335 Ser Gln Cys Thr Asn Leu Lys Cys Pro Arg Arg His Ala Thr Ser Ala 340 345 350 Val Pro Cys Arg Ala Gly Ala Glu Cys Arg Arg Val Asp Cys Thr Phe 355 360 365 Ser His Pro Leu Lys Glu Pro Cys Arg Phe Gly Thr Lys Cys Thr Asn 370 375 380 Lys Val Cys Met Tyr Gln His Pro Glu Gly Arg Thr Ile Ala Ser His 385 390 395 400 Thr Trp Thr Arg Asp Gly Ser Gly Asn Asn Asn Ser Thr Ser Asn Arg 405 410 415 Ser Phe <210> SEQ ID NO 11 <211> LENGTH: 156 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 84 <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/AAD42873 <309> DATABASE ENTRY DATE: 2000-01-05 <313> RELEVANT RESIDUES: (1)..(156) <400> SEQUENCE: 11 Pro Gln Gln Leu His Leu Leu Ser Arg Gln Leu Glu Asp Pro Asn Gly 1 5 10 15 Ser Phe Ser Asn Ala Glu Met Ser Glu Leu Ser Val Ala Gln Lys Pro 20 25 30 Glu Lys Leu Leu Glu Arg Cys Lys Tyr Trp Pro Ala Cys Lys Asn Gly 35 40 45 Asp Glu Cys Ala Tyr His His Pro Ile Ser Pro Cys Lys Ala Phe Pro 50 55 60 Asn Cys Lys Phe Ala Glu Lys Cys Leu Phe Val His Pro Asn Cys Lys 65 70 75 80 Tyr Asp Ala Lys Cys Thr Lys Pro Asp Cys Pro Phe Thr His Val Ser 85 90 95 Arg Arg Ile Gln Leu Cys Arg Tyr Phe Pro Ala Cys Lys Lys Met Glu 100 105 110 Cys Pro Phe Tyr His Pro Lys His Cys Arg Phe Asn Thr Gln Cys Thr 115 120 125 Arg Pro Asp Cys Thr Phe Tyr His Pro Thr Ile Asn Val Pro Pro Arg 130 135 140 His Ala Leu Lys Trp Ile Arg Pro Gln Thr Ser Glu 145 150 155 <210> SEQ ID NO 12 <211> LENGTH: 360 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 85 <400> SEQUENCE: 12 Met Ala Asn Ser Pro Lys Lys Pro Ser Asp Gly Thr Gly Val Ser Ala 1 5 10 15 Ser Asp Thr Pro Lys Tyr Gln His Thr Val Pro Glu Thr Lys Pro Ala 20 25 30 Phe Asn Leu Ser Pro Gly Lys Ala Ser Glu Leu Ser His Ser Leu Pro 35 40 45 Ser Pro Ser Gln Ile Lys Ser Thr Ala His Val Ser Ser Thr His Asn 50 55 60 Asp Ala Ala Gly Asn Thr Asp Asp Ser Val Leu Pro Lys Asn Val Ser 65 70 75 80 Pro Thr Thr Asn Leu Arg Val Glu Ser Asn Gly Asp Thr Asn Asn Met 85 90 95 Phe Ser Ser Pro Ala Gly Leu Ala Leu Pro Lys Lys Asp Asp Lys Lys 100 105 110 Lys Asn Lys Gly Thr Ser Lys Ala Asp Ser Lys Asp Gly Lys Ala Ser 115 120 125 Asn Ser Ser Gly Gln Asn Ala Gln Gln Gln Ser Asp Pro Asn Lys Met 130 135 140 Gln Asp Val Leu Phe Ser Ala Gly Ile Asp Val Arg Glu Glu Glu Ala 145 150 155 160 Leu Leu Asn Ser Ser Ile Asn Ala Ser Lys Ser Gln Val Gln Thr Asn 165 170 175 Asn Val Lys Ile Pro Asn His Leu Pro Phe Leu His Pro Glu Gln Val 180 185 190 Ser Asn Tyr Met Arg Lys Val Gly Lys Glu Gln Asn Phe Asn Leu Thr 195 200 205 Pro Thr Lys Asn Pro Glu Ile Leu Asp Met Met Ser Ser Ala Cys Glu 210 215 220 Asn Tyr Met Arg Asp Ile Leu Thr Asn Ala Ile Val Ile Ser Arg His 225 230 235 240 Arg Arg Lys Ala Val Lys Ile Asn Ser Gly Arg Arg Ser Glu Val Ser 245 250 255 Ala Ala Leu Arg Ala Ile Ala Leu Ile Gln Lys Lys Glu Glu Glu Arg 260 265 270 Arg Val Lys Lys Arg Ile Ala Leu Gly Leu Glu Lys Glu Asp Tyr Glu 275 280 285 Asn Lys Ile Asp Ser Glu Glu Thr Leu His Arg Ala Ser Asn Val Thr 290 295 300 Ala Gly Leu Arg Ala Gly Ser Lys Lys Gln Tyr Gly Trp Leu Thr Ser 305 310 315 320 Ser Val Asn Lys Pro Thr Ser Leu Gly Ala Lys Ser Ser Gly Lys Val 325 330 335 Ala Ser Asp Ile Thr Ala Arg Gly Glu Ser Gly Leu Lys Phe Arg Glu 340 345 350 Ala Arg Glu Glu Pro Gly Ile Val 355 360 <210> SEQ ID NO 13 <211> LENGTH: 358 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 86 <400> SEQUENCE: 13 Met Ser His Lys Ser Met Thr Ser Thr Pro Gln Glu Ser Ser Asn Leu 1 5 10 15 Lys Arg Gln Leu Glu Asn Ser Glu Asp Ser Ser Ser Pro Asn Lys Arg 20 25 30 Ser Lys Thr Glu Thr Thr Thr Glu Asn Gln Ser Ser Trp Glu Ser Asp 35 40 45 Phe Asn Ser Leu Pro Val Glu Leu Leu Gln Thr Glu Thr Asn Gly Thr 50 55 60 Ser Pro Ala Pro Ala Pro Ala Thr Pro Ile Asp Thr Thr Asn Ala Ser 65 70 75 80 Ser Thr Lys Glu Arg Asp Gln Asp Thr Ser Lys Leu Asn Asp Ala Ile 85 90 95 Ala Ala Ala Gly Val Asp Ile Gln Gln Glu Glu Glu Ile Leu Leu Gln 100 105 110 Gln Gln Leu Asn Arg Lys Ser Ala Glu Gly Met Ala Ser Asn Leu Lys 115 120 125 Ser Val Ile Arg Ser Ser Lys Leu Pro Pro Phe Leu His Asn Tyr His 130 135 140 Leu Ala Ala Phe Ile Asp Lys Val Ala Lys Gln Asn Gly Ile Gln Gln 145 150 155 160 Asn Phe Leu Met Asp Gly Glu Met Leu Glu Leu Ile Ser Ala Ala Cys 165 170 175 Glu Thr Trp Leu Ser Asn Leu Ala Thr Lys Thr Ile Ile Leu Ser Arg 180 185 190 His Arg Arg Arg Gly Ile Pro Val Ile Asn Lys Lys Ser Gly Ser Ser 195 200 205 Ser Val Pro Arg Ser Glu Ile Ser Lys Glu Leu Arg Ser Leu Ala Leu 210 215 220 Lys Gln Lys Glu Met Glu Glu Lys Arg Val Asn Lys Arg Val Met Leu 225 230 235 240 Gly Leu Glu Lys Ser Thr Lys Asp Ala Ser Lys Asn Asp Glu Asn Gly 245 250 255 Glu Ser Lys Ala Gly Ala Glu Glu Thr Leu His Arg Ala Ala Asn Ala 260 265 270 Thr Ala Ala Met Met Thr Met Asn Pro Gly Arg Lys Lys Tyr Ser Trp 275 280 285 Met Thr Ser Ser Ala Thr Ala Gly Gly Gly Ser Asp Phe Gly Lys Ser 290 295 300 Ser Gly Gly Ser Ser Lys Asp Ser Gly Lys His Gln Ser Pro Ile Ile 305 310 315 320 Ser Val Arg Gly Asp Asn Gly Leu Arg Phe Arg Glu Ile Arg Ser Gly 325 330 335 Asn Ser Ile Ile Met Lys Asp Leu Leu Gly Ala Ile Glu Asp Glu Lys 340 345 350 Met Gly Thr Arg Asn Ala 355 <210> SEQ ID NO 14 <211> LENGTH: 1023 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 87 <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/CAA72189 <309> DATABASE ENTRY DATE: 1997-06-25 <313> RELEVANT RESIDUES: (1)..(1023) <400> SEQUENCE: 14 Met Ala Ala Gly Ser Asp Leu Leu Asp Glu Val Phe Phe Asn Ser Glu 1 5 10 15 Val Asp Glu Lys Val Val Ser Asp Leu Val Gly Ser Leu Glu Ser Gln 20 25 30 Leu Ala Ala Ser Ala Ala His His His His Leu Ala Pro Arg Thr Pro 35 40 45 Glu Val Arg Ala Ala Ala Ala Gly Ala Leu Gly Asn His Val Val Ser 50 55 60 Gly Ser Pro Ala Gly Ala Ala Gly Ala Gly Pro Ala Ala Pro Ala Glu 65 70 75 80 Gly Ala Pro Gly Ala Ala Pro Glu Pro Pro Pro Ala Gly Arg Ala Arg 85 90 95 Pro Gly Gly Gly Gly Pro Gln Arg Pro Gly Pro Pro Ser Pro Arg Arg 100 105 110 Pro Leu Val Pro Ala Gly Pro Ala Pro Pro Ala Ala Lys Leu Arg Pro 115 120 125 Pro Pro Glu Gly Ser Ala Gly Ala Cys Ala Pro Val Pro Ala Ala Ala 130 135 140 Ala Val Ala Ala Gly Pro Glu Pro Ala Pro Ala Gly Pro Ala Lys Pro 145 150 155 160 Ala Gly Pro Ala Ala Leu Ala Ala Arg Ala Gly Pro Gly Pro Gly Pro 165 170 175 Gly Pro Gly Pro Gly Pro Gly Pro Gly Lys Pro Ala Gly Pro Gly Ala 180 185 190 Ala Gln Thr Leu Asn Gly Ser Ala Ala Leu Leu Asn Ser His His Ala 195 200 205 Ala Ala Pro Ala Val Ser Leu Val Asn Asn Gly Pro Ala Ala Leu Leu 210 215 220 Pro Leu Pro Lys Pro Ala Ala Pro Gly Thr Val Ile Gln Thr Pro Pro 225 230 235 240 Phe Val Gly Ala Ala Ala Pro Pro Ala Pro Ala Ala Pro Ser Pro Pro 245 250 255 Ala Ala Pro Ala Pro Ala Ala Pro Ala Ala Ala Pro Pro Pro Pro Pro 260 265 270 Pro Ala Pro Ala Thr Leu Ala Arg Pro Pro Gly His Pro Ala Gly Pro 275 280 285 Pro Thr Ala Ala Pro Ala Val Pro Pro Pro Ala Ala Ala Gln Asn Gly 290 295 300 Gly Ser Ala Gly Ala Ala Pro Ala Pro Ala Pro Ala Ala Gly Gly Pro 305 310 315 320 Ala Gly Val Ser Gly Gln Pro Gly Pro Gly Ala Ala Ala Ala Ala Pro 325 330 335 Ala Pro Gly Val Lys Ala Glu Ser Pro Lys Arg Val Val Gln Ala Ala 340 345 350 Pro Pro Ala Ala Gln Thr Leu Ala Ala Ser Gly Pro Ala Ser Thr Ala 355 360 365 Ala Ser Met Val Ile Gly Pro Thr Met Gln Gly Ala Leu Pro Ser Pro 370 375 380 Ala Ala Val Pro Pro Pro Ala Pro Gly Thr Pro Thr Gly Leu Pro Lys 385 390 395 400 Gly Ala Ala Gly Ala Val Thr Gln Ser Leu Ser Arg Thr Pro Thr Ala 405 410 415 Thr Thr Ser Gly Ile Arg Ala Thr Leu Thr Pro Thr Val Leu Ala Pro 420 425 430 Arg Leu Pro Gln Pro Pro Gln Asn Pro Thr Asn Ile Gln Asn Phe Gln 435 440 445 Leu Pro Pro Gly Met Val Leu Val Arg Ser Glu Asn Gly Gln Leu Leu 450 455 460 Met Ile Pro Gln Gln Ala Leu Ala Gln Met Gln Ala Gln Ala His Ala 465 470 475 480 Gln Pro Gln Thr Thr Met Ala Pro Arg Pro Ala Thr Pro Thr Ser Ala 485 490 495 Pro Pro Val Gln Ile Ser Thr Val Gln Ala Pro Gly Thr Pro Ile Ile 500 505 510 Ala Arg Gln Val Thr Pro Thr Thr Ile Ile Lys Gln Val Ser Gln Ala 515 520 525 Gln Thr Thr Val Gln Pro Ser Ala Thr Leu Gln Arg Ser Pro Gly Val 530 535 540 Gln Pro Gln Leu Val Leu Gly Gly Ala Ala Gln Thr Ala Ser Leu Gly 545 550 555 560 Thr Ala Thr Ala Val Gln Thr Gly Thr Pro Gln Arg Thr Val Pro Gly 565 570 575 Ala Thr Thr Thr Ser Ser Ala Ala Thr Glu Thr Met Glu Asn Val Lys 580 585 590 Lys Cys Lys Asn Phe Leu Ser Thr Leu Ile Lys Leu Ala Ser Ser Gly 595 600 605 Lys Gln Ser Thr Glu Thr Ala Ala Asn Val Lys Glu Leu Val Gln Asn 610 615 620 Leu Leu Asp Gly Lys Ile Glu Ala Glu Asp Phe Thr Ser Arg Leu Tyr 625 630 635 640 Arg Glu Leu Asn Ser Ser Pro Gln Pro Tyr Leu Val Pro Phe Leu Lys 645 650 655 Arg Ser Leu Pro Ala Leu Arg Gln Leu Thr Pro Asp Ser Ala Ala Phe 660 665 670 Ile Gln Gln Ser Gln Gln Gln Pro Pro Pro Pro Thr Ser Gln Ala Thr 675 680 685 Thr Ala Leu Thr Ala Val Val Leu Ser Ser Ser Val Gln Arg Thr Ala 690 695 700 Gly Lys Thr Ala Ala Thr Val Thr Ser Ala Leu Gln Pro Pro Val Leu 705 710 715 720 Ser Leu Thr Gln Pro Thr Gln Val Gly Val Gly Lys Gln Gly Gln Pro 725 730 735 Thr Pro Leu Val Ile Gln Gln Pro Pro Lys Pro Gly Ala Leu Ile Arg 740 745 750 Pro Pro Gln Val Thr Leu Thr Gln Thr Pro Met Val Ala Leu Arg Gln 755 760 765 Pro His Asn Arg Ile Met Leu Thr Thr Pro Gln Gln Val Asn Leu Ser 770 775 780 Glu Glu Ser Ala Arg Ile Leu Ala Thr Asn Ser Glu Leu Val Gly Thr 785 790 795 800 Leu Thr Arg Ser Cys Lys Asp Glu Thr Phe Leu Leu Gln Ala Pro Leu 805 810 815 Gln Arg Arg Ile Leu Glu Ile Gly Lys Lys His Gly Ile Thr Glu Leu 820 825 830 His Pro Asp Val Val Ser Tyr Val Ser His Ala Thr Gln Gln Arg Leu 835 840 845 Gln Asn Leu Val Glu Lys Ile Ser Glu Thr Ala Gln Gln Lys Asn Phe 850 855 860 Ser Tyr Lys Asp Asp Asp Arg Tyr Glu Gln Ala Ser Asp Val Arg Ala 865 870 875 880 Gln Leu Lys Phe Phe Glu Gln Leu Asp Gln Ile Glu Lys Gln Arg Lys 885 890 895 Asp Glu Gln Glu Arg Glu Ile Leu Met Arg Ala Ala Lys Ser Arg Ser 900 905 910 Arg Gln Glu Asp Pro Glu Gln Leu Arg Leu Lys Gln Lys Ala Lys Glu 915 920 925 Met Gln Gln Gln Glu Leu Ala Gln Met Arg Gln Arg Asp Ala Asn Leu 930 935 940 Thr Ala Leu Ala Ala Ile Gly Pro Arg Lys Lys Arg Lys Val Asp Cys 945 950 955 960 Pro Gly Pro Gly Ser Gly Ala Glu Gly Ser Gly Pro Gly Ser Val Val 965 970 975 Pro Gly Ser Ser Gly Val Gly Thr Pro Arg Gln Phe Thr Arg Gln Arg 980 985 990 Ile Thr Arg Val Asn Leu Arg Asp Leu Ile Phe Cys Leu Glu Asn Glu 995 1000 1005 Arg Glu Thr Ser His Ser Leu Leu Leu Tyr Lys Ala Phe Leu Lys 1010 1015 1020 <210> SEQ ID NO 15 <211> LENGTH: 184 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 88 <400> SEQUENCE: 15 Met Asn Thr Asn Ser Asn Thr Met Val Met Asn Asp Ala Asn Gln Ala 1 5 10 15 Gln Ile Thr Ala Thr Phe Thr Lys Lys Ile Leu Ala His Leu Asp Asp 20 25 30 Pro Asp Ser Asn Lys Leu Ala Gln Phe Val Gln Leu Phe Asn Pro Asn 35 40 45 Asn Cys Arg Ile Ile Phe Asn Ala Thr Pro Phe Ala Gln Ala Thr Val 50 55 60 Phe Leu Gln Met Trp Gln Asn Gln Val Val Gln Thr Gln His Ala Leu 65 70 75 80 Thr Gly Val Asp Tyr His Ala Ile Pro Gly Ser Gly Thr Leu Ile Cys 85 90 95 Asn Val Asn Cys Lys Val Arg Phe Asp Glu Ser Gly Arg Asp Lys Met 100 105 110 Gly Gln Asp Ala Thr Val Pro Ile Gln Pro Asn Asn Thr Gly Asn Arg 115 120 125 Asn Arg Pro Asn Asp Met Asn Lys Pro Arg Pro Leu Trp Gly Pro Tyr 130 135 140 Phe Gly Ile Ser Leu Gln Leu Ile Ile Asp Asp Arg Ile Phe Arg Asn 145 150 155 160 Asp Phe Asn Gly Val Ile Ser Gly Phe Asn Tyr Asn Met Val Tyr Lys 165 170 175 Pro Glu Asp Ser Leu Leu Lys Ile 180 <210> SEQ ID NO 16 <211> LENGTH: 181 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 89 <400> SEQUENCE: 16 Met Asn Gln Asp Pro Thr Gln Gln Leu Glu Pro Phe Leu Lys Arg Phe 1 5 10 15 Leu Ala Ser Leu Asp Leu Leu Tyr Thr Gln Pro Thr Ser Gln Pro Phe 20 25 30 Pro Asn Val Glu Ser Tyr Ala Thr Gln Leu Gly Ser Asn Leu Lys Arg 35 40 45 Ser Ser Ala Ile Ile Val Asn Gly Gln Pro Ile Ile Pro Ser Pro Gln 50 55 60 Glu Asp Cys Lys Leu Gln Phe Gln Lys Lys Trp Leu Gln Thr Pro Leu 65 70 75 80 Ser Ser His Gln Leu Thr Ser Tyr Asp Gly His Leu Ile Pro Gly Thr 85 90 95 Gly Thr Phe Val Val His Phe Ser Ala Lys Val Arg Phe Asp Gln Ser 100 105 110 Gly Arg Asn Arg Leu Gly Glu Ser Ala Asp Leu Phe Gln Glu Asn Asn 115 120 125 Ser Ile Val Ser Lys Thr Asn Gln Arg Pro Ile Trp Gly Ser Trp Phe 130 135 140 Gly Val Asp Val Asn Leu Val Val Asp Glu Asn Val Met Gln Asp Gly 145 150 155 160 Glu Ile Ile Asn Ser Met Asp Tyr Arg Phe Thr Tyr Val Pro Asn Asp 165 170 175 Ser Ile Ile Lys Val 180 <210> SEQ ID NO 17 <211> LENGTH: 244 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 90 <400> SEQUENCE: 17 Met Asn Ala Leu Tyr Asn His Ala Val Lys Gln Lys Asn Gln Leu Gln 1 5 10 15 Gln Glu Leu Ala Arg Phe Glu Lys Asn Ser Val Thr Ala Pro Ile Ser 20 25 30 Leu Gln Gly Ser Ile Ser Ala Thr Leu Val Ser Leu Glu Lys Thr Val 35 40 45 Lys Gln Tyr Ala Glu His Leu Asn Arg Tyr Lys Glu Asp Thr Asn Ala 50 55 60 Glu Glu Ile Asp Pro Lys Phe Ala Asn Arg Leu Ala Thr Leu Thr Gln 65 70 75 80 Asp Leu His Asp Phe Thr Ala Lys Phe Lys Asp Leu Lys Gln Ser Tyr 85 90 95 Asn Glu Asn Asn Ser Arg Thr Gln Leu Phe Gly Ser Gly Ala Ser His 100 105 110 Val Met Asp Ser Asp Asn Pro Phe Ser Thr Ser Glu Thr Ile Met Asn 115 120 125 Lys Arg Asn Val Gly Gly Ala Ser Ala Asn Gly Lys Glu Gly Ser Ser 130 135 140 Asn Gly Gly Gly Leu Pro Leu Tyr Gln Gly Leu Gln Lys Glu Gln Ser 145 150 155 160 Val Phe Glu Arg Gly Asn Ala Gln Leu Asp Tyr Ile Leu Glu Met Gly 165 170 175 Gln Gln Ser Phe Glu Asn Ile Val Glu Gln Asn Lys Ile Leu Ser Lys 180 185 190 Val Gln Asp Arg Met Ser Asn Gly Leu Arg Thr Leu Gly Val Ser Glu 195 200 205 Gln Thr Ile Thr Ser Ile Asn Lys Arg Val Phe Lys Asp Lys Leu Val 210 215 220 Phe Trp Ile Ala Leu Ile Leu Leu Ile Ile Gly Ile Tyr Tyr Val Leu 225 230 235 240 Lys Trp Leu Arg <210> SEQ ID NO 18 <211> LENGTH: 238 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 91 <400> SEQUENCE: 18 Met Asn Ser Ile Tyr Asn His Gly Leu Lys Gln Thr Gln Thr Ile Thr 1 5 10 15 Lys Asp Leu Thr Gln Phe Glu Lys Asn Leu Ser Thr Ser Pro Leu Ser 20 25 30 Leu Gln Gly Ala Ile Thr Thr Ser Leu Thr Ala Phe Arg Lys Thr Ile 35 40 45 Lys Glu Tyr Ser Asp Leu Leu Glu Lys Asn Val Asn Asp Thr Ser Tyr 50 55 60 Thr Lys His Glu Asn Arg Leu Asn Lys Phe Asn Gln Asp Leu Asn Glu 65 70 75 80 Phe Thr Leu Lys Phe Asp Thr Leu Lys Lys Gln Arg Asp Ile Gln Val 85 90 95 Gln Glu Ala Asn Lys Gln Glu Leu Leu Gly Arg Arg His Ile Ser Thr 100 105 110 Thr Ala Thr Ala Ala Leu Gly Ser Thr Ser Ser Asp Asn Pro Tyr Glu 115 120 125 Ser Ser Ser Asn Pro Ser Gln Gln Gln Gln Gln Gln Leu Gln Asp Glu 130 135 140 Gln Asn Thr Met Ser Tyr Arg Glu Gly Leu Tyr His Glu Lys Asn Ser 145 150 155 160 Leu Glu Arg Gly Ser Glu Gln Leu Asp Arg Ile Leu Glu Met Gly Gln 165 170 175 Gln Ala Phe Glu Asp Ile Val Glu Gln Asn Glu Ile Leu Arg Lys Val 180 185 190 Gln Thr Lys Phe Glu Glu Ser Leu Ile Thr Leu Gly Val Ser Gln Gly 195 200 205 Thr Ile Arg Ser Val Glu Arg Arg Ala Lys Gln Asp Lys Trp Leu Phe 210 215 220 Trp Phe Cys Val Val Val Met Leu Val Val Phe Tyr Tyr Ile 225 230 235 <210> SEQ ID NO 19 <211> LENGTH: 261 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 92 <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/NP_003560 <309> DATABASE ENTRY DATE: 2000-11-01 <313> RELEVANT RESIDUES: (1)..(261) <400> SEQUENCE: 19 Met Ser Tyr Thr Pro Gly Val Gly Gly Asp Pro Thr Gln Leu Ala Gln 1 5 10 15 Arg Ile Ser Ser Asn Ile Gln Lys Ile Thr Gln Cys Ser Val Glu Ile 20 25 30 Gln Arg Thr Leu Asn Gln Leu Gly Thr Pro Gln Asp Ser Pro Glu Leu 35 40 45 Arg Gln Gln Leu Gln Gln Lys Gln Gln Tyr Thr Asn Gln Leu Ala Lys 50 55 60 Glu Thr Asp Lys Tyr Ile Lys Glu Phe Gly Ser Leu Pro Thr Thr Pro 65 70 75 80 Ser Glu Gln Arg Gln Arg Lys Ile Gln Lys Asp Arg Leu Val Ala Glu 85 90 95 Phe Thr Thr Ser Leu Thr Asn Phe Gln Lys Val Gln Arg Gln Ala Ala 100 105 110 Glu Arg Glu Lys Glu Phe Val Ala Arg Val Arg Ala Ser Ser Arg Val 115 120 125 Ser Gly Ser Phe Pro Glu Asp Ser Ser Lys Glu Arg Asn Leu Val Ser 130 135 140 Trp Glu Ser Gln Thr Gln Pro Gln Val Gln Val Gln Asp Glu Glu Ile 145 150 155 160 Thr Glu Asp Asp Leu Arg Leu Ile His Glu Arg Glu Ser Ser Ile Arg 165 170 175 Gln Leu Glu Ala Asp Ile Met Asp Ile Asn Glu Ile Phe Lys Asp Leu 180 185 190 Gly Met Met Ile His Glu Gln Gly Asp Val Ile Asp Ser Ile Glu Ala 195 200 205 Asn Val Glu Asn Ala Glu Val His Val Gln Gln Ala Asn Gln Gln Leu 210 215 220 Ser Arg Ala Ala Asp Tyr Gln Arg Lys Ser Arg Lys Thr Leu Cys Ile 225 230 235 240 Ile Ile Leu Ile Leu Val Ile Gly Val Ala Ile Ile Ser Leu Ile Ile 245 250 255 Trp Gly Leu Asn His 260 <210> SEQ ID NO 20 <211> LENGTH: 258 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 93 <300> PUBLICATION INFORMATION: <301> AUTHORS: Bauer and Burgers <302> TITLE: Molecular cloning, structure and expression of the yeast proliferating cell nuclear antigen gene. <303> JOURNAL: Nucleic Acids Research <304> VOLUME: 18 <305> ISSUE: 2 <306> PAGES: 261-265 <307> DATE: 1990 <308> DATABASE ACCESSION NUMBER: X16676 <309> DATABASE ENTRY DATE: 1993-09-30 <400> SEQUENCE: 20 Met Leu Glu Ala Lys Phe Glu Glu Ala Ser Leu Phe Lys Arg Ile Ile 1 5 10 15 Asp Gly Phe Lys Asp Cys Val Gln Leu Val Asn Phe Gln Cys Lys Glu 20 25 30 Asp Gly Ile Ile Ala Gln Ala Val Asp Asp Ser Arg Val Leu Leu Val 35 40 45 Ser Leu Glu Ile Gly Val Glu Ala Phe Gln Glu Tyr Arg Cys Asp His 50 55 60 Pro Val Thr Leu Gly Met Asp Leu Thr Ser Leu Ser Lys Ile Leu Arg 65 70 75 80 Cys Gly Asn Asn Thr Asp Thr Leu Thr Leu Ile Ala Asp Asn Thr Pro 85 90 95 Asp Ser Ile Ile Leu Leu Phe Glu Asp Thr Lys Lys Asp Arg Ile Ala 100 105 110 Glu Tyr Ser Leu Lys Leu Met Asp Ile Asp Ala Asp Phe Leu Lys Ile 115 120 125 Glu Glu Leu Gln Tyr Asp Ser Thr Leu Ser Leu Pro Ser Ser Glu Phe 130 135 140 Ser Lys Ile Val Arg Asp Leu Ser Gln Leu Ser Asp Ser Ile Asn Ile 145 150 155 160 Met Ile Thr Lys Glu Thr Ile Lys Phe Val Ala Asp Gly Asp Ile Gly 165 170 175 Ser Gly Ser Val Ile Ile Lys Pro Phe Val Asp Met Glu His Pro Glu 180 185 190 Thr Ser Ile Lys Leu Glu Met Asp Gln Pro Val Asp Leu Thr Phe Gly 195 200 205 Ala Lys Tyr Leu Leu Asp Ile Ile Lys Gly Ser Ser Leu Ser Asp Arg 210 215 220 Val Gly Ile Arg Leu Ser Ser Glu Ala Pro Ala Leu Phe Gln Phe Asp 225 230 235 240 Leu Lys Ser Gly Phe Leu Gln Phe Phe Leu Ala Pro Lys Phe Asn Asp 245 250 255 Glu Glu <210> SEQ ID NO 21 <211> LENGTH: 259 <212> TYPE: PRT <213> ORGANISM: Canidia albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 94 <400> SEQUENCE: 21 Met Leu Glu Gly Lys Phe Glu Glu Ala Ala Leu Leu Lys Lys Val Val 1 5 10 15 Glu Ala Ile Lys Asp Cys Val Lys Lys Cys Asn Phe Asn Cys Ser Glu 20 25 30 His Gly Ile Thr Val Gln Ala Val Asp Asp Ser Arg Val Leu Leu Val 35 40 45 Ser Leu Leu Ile Gly Gln Thr Ser Phe Ser Glu Arg Cys Asp Arg Asp 50 55 60 Val Thr Leu Gly Ile Asp Leu Glu Ser Phe Ser Lys Ile Ile Lys Ser 65 70 75 80 Ala Asn Asn Glu Asp Phe Leu Thr Leu Leu Ala Glu Asp Ser Pro Asp 85 90 95 Gln Ile Met Ala Ile Leu Glu Glu Lys Gln Lys Glu Lys Ile Ser Glu 100 105 110 Tyr Ser Leu Lys Leu Met Asp Ile Asp Ser Glu Phe Leu Gln Ile Asp 115 120 125 Asp Met Glu Tyr Asp Ala Val Val Asn Met Pro Ser Ser Asp Phe Ala 130 135 140 Lys Leu Val Arg Asp Leu Lys Asn Leu Ser Glu Ser Leu Arg Val Val 145 150 155 160 Val Thr Lys Asp Ser Val Lys Phe Thr Ser Glu Gly Asp Ser Gly Ser 165 170 175 Gly Ser Val Ile Leu Lys Pro Tyr Thr Asn Leu Lys Asn Glu Arg Glu 180 185 190 Ser Val Thr Ile Ser Leu Asp Asp Pro Val Asp Leu Thr Phe Gly Leu 195 200 205 Lys Tyr Leu Asn Asp Ile Val Lys Ala Ala Thr Leu Ser Asp Val Ile 210 215 220 Thr Ile Lys Leu Ala Asp Lys Thr Pro Ala Leu Phe Glu Phe Lys Met 225 230 235 240 Gln Ser Gly Gly Tyr Leu Arg Phe Tyr Leu Ala Pro Lys Phe Asp Asp 245 250 255 Asp Glu Tyr <210> SEQ ID NO 22 <211> LENGTH: 261 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 95 <300> PUBLICATION INFORMATION: <301> AUTHORS: Almendral, Huebsch, Blundell, MacDonald-Bravo, and Bravo <302> TITLE: Cloning and sequence of the human nuclear protein cyclin: Homology with DNA-binding proteins <303> JOURNAL: Proc. Natl. Acad. Sci. U.S.A. <304> VOLUME: 84 <305> ISSUE: 6 <306> PAGES: 1575-1579 <307> DATE: 1987 <308> DATABASE ACCESSION NUMBER: m15796 <309> DATABASE ENTRY DATE: 1993-04-27 <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/P12004 <309> DATABASE ENTRY DATE: 2001-10-16 <313> RELEVANT RESIDUES: (1)..(261) <400> SEQUENCE: 22 Met Phe Glu Ala Arg Leu Val Gln Gly Ser Ile Leu Lys Lys Val Leu 1 5 10 15 Glu Ala Leu Lys Asp Leu Ile Asn Glu Ala Cys Trp Asp Ile Ser Ser 20 25 30 Ser Gly Val Asn Leu Gln Ser Met Asp Ser Ser His Val Ser Leu Val 35 40 45 Gln Leu Thr Leu Arg Ser Glu Gly Phe Asp Thr Tyr Arg Cys Asp Arg 50 55 60 Asn Leu Ala Met Gly Val Asn Leu Thr Ser Met Ser Lys Ile Leu Lys 65 70 75 80 Cys Ala Gly Asn Glu Asp Ile Ile Thr Leu Arg Ala Glu Asp Asn Ala 85 90 95 Asp Thr Leu Ala Leu Val Phe Glu Ala Pro Asn Gln Glu Lys Val Ser 100 105 110 Asp Tyr Glu Met Lys Leu Met Asp Leu Asp Val Glu Gln Leu Gly Ile 115 120 125 Pro Glu Gln Glu Tyr Ser Cys Val Val Lys Met Pro Ser Gly Glu Phe 130 135 140 Ala Arg Ile Cys Arg Asp Leu Ser His Ile Gly Asp Ala Val Val Ile 145 150 155 160 Ser Cys Ala Lys Asp Gly Val Lys Phe Ser Ala Ser Gly Glu Leu Gly 165 170 175 Asn Gly Asn Ile Lys Leu Ser Gln Thr Ser Asn Val Asp Lys Glu Glu 180 185 190 Glu Ala Val Thr Ile Glu Met Asn Glu Pro Val Gln Leu Thr Phe Ala 195 200 205 Leu Arg Tyr Leu Asn Phe Phe Thr Lys Ala Thr Pro Leu Ser Ser Thr 210 215 220 Val Thr Leu Ser Met Ser Ala Asp Val Pro Leu Val Val Glu Tyr Lys 225 230 235 240 Ile Ala Asp Met Gly His Leu Lys Tyr Tyr Leu Ala Pro Lys Ile Glu 245 250 255 Asp Glu Glu Gly Ser 260 <210> SEQ ID NO 23 <211> LENGTH: 511 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 96 <400> SEQUENCE: 23 Met Ser Lys Arg Ser Ile Glu Val Asn Glu Glu Gln Asp Arg Val Val 1 5 10 15 Ser Ala Lys Thr Glu Ser His Ser Val Pro Ala Ile Pro Ala Ser Glu 20 25 30 Glu Gln Asp Ala Pro Lys Asn Asp Leu Glu Glu Gln Leu Ser Asp Glu 35 40 45 Phe Asp Ser Asp Gly Glu Ile Ile Glu Ile Asp Gly Asp Asp Glu Ile 50 55 60 Asn Asp Glu Asp Asp Leu Arg Lys Lys Gln Glu Glu Ala Glu Thr Leu 65 70 75 80 Val Gln Lys Asp Gln Ser Glu Gly Asn Lys Glu Lys Ile Gln Glu Leu 85 90 95 Tyr Leu Pro His Met Ser Arg Pro Leu Gly Pro Asp Glu Val Leu Glu 100 105 110 Ala Asp Pro Thr Val Tyr Glu Met Leu His Asn Val Asn Met Pro Trp 115 120 125 Pro Cys Leu Thr Leu Asp Val Ile Pro Asp Thr Leu Gly Ser Glu Arg 130 135 140 Arg Asn Tyr Pro Gln Ser Ile Leu Leu Thr Thr Ala Thr Gln Ser Ser 145 150 155 160 Arg Lys Lys Glu Asn Glu Leu Met Val Leu Ala Leu Ser Asn Leu Ala 165 170 175 Lys Thr Leu Leu Lys Asp Asp Asn Glu Gly Glu Asp Asp Glu Glu Asp 180 185 190 Asp Glu Asp Asp Val Asp Pro Val Ile Glu Asn Glu Asn Ile Pro Leu 195 200 205 Arg Asp Thr Thr Asn Arg Leu Lys Val Ser Pro Phe Ala Ile Ser Asn 210 215 220 Gln Glu Val Leu Thr Ala Thr Met Ser Glu Asn Gly Asp Val Tyr Ile 225 230 235 240 Tyr Asn Leu Ala Pro Gln Ser Lys Ala Phe Ser Thr Pro Gly Tyr Gln 245 250 255 Ile Pro Lys Ser Ala Lys Arg Pro Ile His Thr Val Lys Asn His Gly 260 265 270 Asn Val Glu Gly Tyr Gly Leu Asp Trp Ser Pro Leu Ile Lys Thr Gly 275 280 285 Ala Leu Leu Ser Gly Asp Cys Ser Gly Gln Ile Tyr Phe Thr Gln Arg 290 295 300 His Thr Ser Arg Trp Val Thr Asp Lys Gln Pro Phe Thr Val Ser Asn 305 310 315 320 Asn Lys Ser Ile Glu Asp Ile Gln Trp Ser Arg Thr Glu Ser Thr Val 325 330 335 Phe Ala Thr Ala Gly Cys Asp Gly Tyr Ile Arg Ile Trp Asp Thr Arg 340 345 350 Ser Lys Lys His Lys Pro Ala Ile Ser Val Lys Ala Ser Asn Thr Asp 355 360 365 Val Asn Val Ile Ser Trp Ser Asp Lys Ile Gly Tyr Leu Leu Ala Ser 370 375 380 Gly Asp Asp Asn Gly Thr Trp Gly Val Trp Asp Leu Arg Gln Phe Thr 385 390 395 400 Pro Ser Asn Ala Asp Ala Val Gln Pro Val Ala Gln Tyr Asp Phe His 405 410 415 Lys Gly Ala Ile Thr Ser Ile Ala Phe Asn Pro Leu Asp Glu Ser Ile 420 425 430 Val Ala Val Gly Ser Glu Asp Asn Thr Val Thr Leu Trp Asp Leu Ser 435 440 445 Val Glu Ala Asp Asp Glu Glu Ile Lys Gln Gln Ala Ala Glu Thr Lys 450 455 460 Glu Leu Gln Glu Ile Pro Pro Gln Leu Leu Phe Val His Trp Gln Lys 465 470 475 480 Glu Val Lys Asp Val Lys Trp His Lys Gln Ile Pro Gly Cys Leu Val 485 490 495 Ser Thr Gly Thr Asp Gly Leu Asn Val Trp Lys Thr Ile Ser Val 500 505 510 <210> SEQ ID NO 24 <211> LENGTH: 420 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 97 <400> SEQUENCE: 24 Met Ser Lys Arg Ser Ala Glu Asp Asp Leu Ser Gly Asn Gly Ser Thr 1 5 10 15 Ser His Thr Ala Val Lys Thr Asn Lys Asp Ser Leu Pro Thr Thr Thr 20 25 30 Asn Gly Lys Glu Glu Glu Pro Asp Asn Met Asp Ile Gly Glu Phe Glu 35 40 45 Asp Pro Tyr Gly Asp Glu Phe Glu Ser Asp Glu Ile Ile Glu Leu Asp 50 55 60 Asp Asn Asn Asp Glu Glu Asp Asp Glu Met Ile Asp Glu Asn Ser Thr 65 70 75 80 Gln Ala Lys Ile Glu Glu Leu Glu Ala Lys Glu Gln Glu Gln Glu Gln 85 90 95 Gln Ser Ser Ile Tyr Leu Pro His Lys Ser Lys Pro Leu Gly Pro Asp 100 105 110 Glu Val Leu Glu Ala Asp Pro Thr Val Tyr Glu Met Leu His Asn Ile 115 120 125 Asn Leu Pro Trp Pro Cys Leu Thr Val Asp Ile Leu Pro Asp Ser Leu 130 135 140 Gly Asn Glu Arg Arg Ser Tyr Pro Ala Thr Val Tyr Leu Ala Thr Ala 145 150 155 160 Thr Gln Ala Ala Lys Ala Lys Asp Asn Glu Leu Leu Ala Met Lys Ala 165 170 175 Ser Ser Leu Ala Lys Thr Leu Val Lys Asp Glu Asn Glu Glu Asp Glu 180 185 190 Glu Asp Glu Asp Asp Asp Asp Asp Val Asp Ser Asp Pro Ile Leu Asp 195 200 205 Ser Glu Ser Ile Pro Leu Arg His Thr Thr Asn Arg Ile Arg Val Ser 210 215 220 Pro His Ala Gln Gln Thr Gly Glu Tyr Leu Thr Ala Ser Met Ser Glu 225 230 235 240 Asn Gly Glu Val Tyr Ile Phe Asp Leu Leu Ala Gln Tyr Lys Ala Phe 245 250 255 Asp Thr Pro Gly Tyr Met Ile Pro Lys Ser Ser Lys Arg Pro Ile His 260 265 270 Thr Ile Arg Ala His Gly Asn Val Glu Gly Tyr Gly Leu Asp Trp Ser 275 280 285 Pro Leu Val Asn Thr Gly Ala Leu Leu Ser Gly Asp Met Ser Gly Arg 290 295 300 Ile Tyr Leu Thr Asn Arg Thr Thr Ser Ser Trp Thr Thr Asp Lys Thr 305 310 315 320 Pro Phe Phe Ala Ser Gln Ser Ser Ile Glu Asp Ile Gln Trp Ser Thr 325 330 335 Gly Glu Thr Thr Val Phe Ala Thr Gly Gly Cys Asp Gly Tyr Ile Cys 340 345 350 Ile Trp Asp Thr Arg Ser Lys Lys His Lys Pro Ala Leu Ser Val Ile 355 360 365 Ala Ser Lys Ser Asp Val Asn Val Ile Ser Trp Ser Ser Lys Ile Asn 370 375 380 His Leu Leu Ala Ser Gly His Asp Asp Gly Ser Trp Gly Val Trp Asp 385 390 395 400 Leu Arg Asn Phe Thr Asn Asn Thr Thr Ser Asn Pro Ser Pro Val Ala 405 410 415 Asn Tyr Asp Phe 420 <210> SEQ ID NO 25 <211> LENGTH: 425 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 98 <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/NP_005601 <309> DATABASE ENTRY DATE: 2001-12-20 <313> RELEVANT RESIDUES: (1)..(425) <400> SEQUENCE: 25 Met Ala Asp Lys Glu Ala Ala Phe Asp Asp Ala Val Glu Glu Arg Val 1 5 10 15 Ile Asn Glu Glu Tyr Lys Ile Trp Lys Lys Asn Thr Pro Phe Leu Tyr 20 25 30 Asp Leu Val Met Thr His Ala Leu Glu Trp Pro Ser Leu Thr Ala Gln 35 40 45 Trp Leu Pro Asp Val Thr Arg Pro Glu Gly Lys Asp Phe Ser Ile His 50 55 60 Arg Leu Val Leu Gly Thr His Thr Ser Asp Glu Gln Asn His Leu Val 65 70 75 80 Ile Ala Ser Val Gln Leu Pro Asn Asp Asp Ala Gln Phe Asp Ala Ser 85 90 95 His Tyr Asp Ser Glu Lys Gly Glu Phe Gly Gly Phe Gly Ser Val Ser 100 105 110 Gly Lys Ile Glu Ile Glu Ile Lys Ile Asn His Glu Gly Glu Val Asn 115 120 125 Arg Ala Arg Tyr Met Pro Gln Asn Pro Cys Ile Ile Ala Thr Lys Thr 130 135 140 Pro Ser Ser Asp Val Leu Val Phe Asp Tyr Thr Lys His Pro Ser Lys 145 150 155 160 Pro Asp Pro Ser Gly Glu Cys Asn Pro Asp Leu Arg Leu Arg Gly His 165 170 175 Gln Lys Glu Gly Tyr Gly Leu Ser Trp Asn Pro Asn Leu Ser Gly His 180 185 190 Leu Leu Ser Ala Ser Asp Asp His Thr Ile Cys Leu Trp Asp Ile Ser 195 200 205 Ala Val Pro Lys Glu Gly Lys Val Val Asp Ala Lys Thr Ile Phe Thr 210 215 220 Gly His Thr Ala Val Val Glu Asp Val Ser Trp His Leu Leu His Glu 225 230 235 240 Ser Leu Phe Gly Ser Val Ala Asp Asp Gln Lys Leu Met Ile Trp Asp 245 250 255 Thr Arg Ser Asn Asn Thr Ser Lys Pro Ser His Ser Val Asp Ala His 260 265 270 Thr Ala Glu Val Asn Cys Leu Ser Phe Asn Pro Tyr Ser Glu Phe Ile 275 280 285 Leu Ala Thr Gly Ser Ala Asp Lys Thr Val Ala Leu Trp Asp Leu Arg 290 295 300 Asn Leu Lys Leu Lys Leu His Ser Phe Glu Ser His Lys Asp Glu Ile 305 310 315 320 Phe Gln Val Gln Trp Ser Pro His Asn Glu Thr Ile Leu Ala Ser Ser 325 330 335 Gly Thr Asp Arg Arg Leu Asn Val Trp Asp Leu Ser Lys Ile Gly Glu 340 345 350 Glu Gln Ser Pro Glu Asp Ala Glu Asp Gly Pro Pro Glu Leu Leu Phe 355 360 365 Ile His Gly Gly His Thr Ala Lys Ile Ser Asp Phe Ser Trp Asn Pro 370 375 380 Asn Glu Pro Trp Val Ile Cys Ser Val Ser Glu Asp Asn Ile Met Gln 385 390 395 400 Val Trp Gln Met Ala Glu Asn Ile Tyr Asn Asp Glu Asp Pro Glu Gly 405 410 415 Ser Val Asp Pro Glu Gly Gln Gly Ser 420 425 <210> SEQ ID NO 26 <211> LENGTH: 431 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 99 <400> SEQUENCE: 26 Met Glu Pro Gln Glu Glu Phe Ile Thr Thr Glu Glu Val Glu Gln Glu 1 5 10 15 Ile Val Pro Thr Val Glu Val Glu Gln Asp Val Pro Val Asp Ile Glu 20 25 30 Gly Glu Asn Asp Asp Asp Asp Glu Met Met Asn Asp Asp Glu Glu Ala 35 40 45 Leu Glu Val Asp Met Ser Asn Asn Ser Leu Thr Tyr Phe Asp Lys His 50 55 60 Thr Asp Ser Val Phe Ala Ile Gly His His Pro Asn Leu Pro Leu Val 65 70 75 80 Cys Thr Gly Gly Gly Asp Asn Leu Ala His Leu Trp Thr Ser His Ser 85 90 95 Gln Pro Pro Lys Phe Ala Gly Thr Leu Thr Gly Tyr Gly Glu Ser Val 100 105 110 Ile Ser Cys Ser Phe Thr Ser Glu Gly Gly Phe Leu Val Thr Ala Asp 115 120 125 Met Ser Gly Lys Val Leu Val His Met Gly Gln Lys Gly Gly Ala Gln 130 135 140 Trp Lys Leu Ala Ser Gln Met Gln Glu Val Glu Glu Ile Val Trp Leu 145 150 155 160 Lys Thr His Pro Thr Ile Ala Arg Thr Phe Ala Phe Gly Ala Thr Asp 165 170 175 Gly Ser Val Trp Cys Tyr Gln Ile Asn Glu Gln Asp Gly Ser Leu Glu 180 185 190 Gln Leu Met Ser Gly Phe Val His Gln Gln Asp Cys Ser Met Gly Glu 195 200 205 Phe Ile Asn Thr Asp Lys Gly Glu Asn Thr Leu Glu Leu Val Thr Cys 210 215 220 Ser Leu Asp Ser Thr Ile Val Ala Trp Asn Cys Phe Thr Gly Gln Gln 225 230 235 240 Leu Phe Lys Ile Thr Gln Ala Glu Ile Lys Gly Leu Glu Ala Pro Trp 245 250 255 Ile Ser Leu Ser Leu Ala Pro Glu Thr Leu Thr Lys Gly Asn Ser Gly 260 265 270 Val Val Ala Cys Gly Ser Asn Asn Gly Leu Leu Ala Val Ile Asn Cys 275 280 285 Asn Asn Gly Gly Ala Ile Leu His Leu Ser Thr Val Ile Glu Leu Lys 290 295 300 Pro Glu Gln Asp Glu Leu Asp Ala Ser Ile Glu Ser Ile Ser Trp Ser 305 310 315 320 Ser Lys Phe Ser Leu Met Ala Ile Gly Leu Val Cys Gly Glu Ile Leu 325 330 335 Leu Tyr Asp Thr Ser Ala Trp Arg Val Arg His Lys Phe Val Leu Glu 340 345 350 Asp Ser Val Thr Lys Leu Met Phe Asp Asn Asp Asp Leu Phe Ala Ser 355 360 365 Cys Ile Asn Gly Lys Val Tyr Gln Phe Asn Ala Arg Thr Gly Gln Glu 370 375 380 Lys Phe Val Cys Val Gly His Asn Met Gly Val Leu Asp Phe Ile Leu 385 390 395 400 Leu His Pro Val Ala Asn Thr Gly Thr Glu Gln Lys Arg Lys Val Ile 405 410 415 Thr Ala Gly Asp Glu Gly Val Ser Leu Val Phe Glu Val Pro Asn 420 425 430 <210> SEQ ID NO 27 <211> LENGTH: 417 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: MISC_FEATURE <222> LOCATION: (326)..(326) <223> OTHER INFORMATION: X can be any amino acid <220> FEATURE: <221> NAME/KEY: MISC_FEATURE <222> LOCATION: (367)..(367) <223> OTHER INFORMATION: X can be any amino acid <220> FEATURE: <221> NAME/KEY: MISC_FEATURE <222> LOCATION: (378)..(378) <223> OTHER INFORMATION: X can be any amino acid <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 100 <400> SEQUENCE: 27 Met Ser His Gln Gln Glu Asp Val Val Asp Asp Thr Gln Glu Glu Tyr 1 5 10 15 Ile Asn Val Asn Glu Val Ala Glu Glu Val Ala Asp Asp Asp Gln Ala 20 25 30 Pro Pro Asp Glu Glu Asp Glu Glu Met Glu Leu Asp Asp Glu His Glu 35 40 45 Thr Leu Glu Ile Asp Met Ser Asn Asn Ser Trp Thr Tyr Phe Asp Lys 50 55 60 His Thr Asp Ser Ile Phe Thr Ile Phe Ser His Pro Lys Leu Pro Met 65 70 75 80 Val Leu Thr Glu Gly Gly Asp Asn Thr Ala Tyr Leu Trp Thr Thr His 85 90 95 Thr Gln Pro Pro Arg Phe Val Gly Glu Ile Thr Gly His Lys Glu Ser 100 105 110 Val Ile Ser Gly Gly Phe Thr Ala Asp Gly Lys Phe Val Val Thr Ala 115 120 125 Asp Met Asn Gly Leu Ile Gln Val Phe Lys Ala Thr Lys Gly Gly Glu 130 135 140 Gln Trp Val Lys Phe Gly Glu Leu Asp Glu Val Glu Glu Val Leu Phe 145 150 155 160 Val Thr Val His Pro Thr Leu Pro Phe Phe Ala Phe Gly Ala Thr Asp 165 170 175 Gly Ser Ile Trp Val Tyr Gln Ile Asp Glu Ser Ser Lys Leu Leu Val 180 185 190 Gln Ile Met Ser Gly Phe Ser His Thr Leu Lys Cys Asn Gly Ala Val 195 200 205 Phe Ile Gln Gly Lys Asp Glu Asn Asp Leu Thr Leu Val Ser Ile Ser 210 215 220 Glu Asp Gly Thr Val Val Asn Trp Asn Cys Phe Thr Gly Gln Val Asn 225 230 235 240 Tyr Lys Leu Gln Pro His Asp Asp Phe Lys Gly Val Glu Ser Pro Trp 245 250 255 Val Thr Val Lys Val His Gly Asn Leu Val Ala Ile Gly Gly Arg Asp 260 265 270 Gly Gln Leu Ser Ile Val Asn Asn Asp Thr Gly Lys Ile Val His Thr 275 280 285 Leu Lys Thr Leu Asp Asn Val Asp Asp Ile Ala Glu Leu Ser Ile Glu 290 295 300 Ala Leu Ser Trp Cys Glu Ser Lys Asn Ile Asn Leu Leu Ala Val Gly 305 310 315 320 Leu Val Ser Gly Asp Xaa Leu Leu Phe Asp Thr Gln Gln Trp Arg Leu 325 330 335 Arg Lys Asn Leu Lys Val Asp Asp Ala Ile Thr Lys Leu Gln Phe Val 340 345 350 Gly Glu Thr Pro Ile Leu Val Gly Asn Ser Met Asp Gly Lys Xaa Tyr 355 360 365 Lys Trp Glu Pro Arg Thr Gly Glu Lys Xaa Phe Ala Gly Val Gly Thr 370 375 380 Asn Met Gly Ser Tyr Gly Leu Cys Tyr Phe Lys Ile Glu Val Lys Asn 385 390 395 400 Trp Leu Leu Leu Val Asp Glu Arg Cys Phe His Trp Ser Leu Phe Met 405 410 415 Lys <210> SEQ ID NO 28 <211> LENGTH: 611 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 101 <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/NP_001078 <309> DATABASE ENTRY DATE: 2001-12-18 <313> RELEVANT RESIDUES: (1)..(611) <400> SEQUENCE: 28 Met Asp Ser Gly Arg Arg Leu Gly Pro Glu Lys Trp Ile Arg Arg Leu 1 5 10 15 Arg Arg Met Glu Ser Glu Ser Glu Ser Gly Ala Ala Ala Asp Thr Pro 20 25 30 Pro Leu Glu Thr Leu Ser Phe His Gly Asp Glu Glu Ile Ile Glu Val 35 40 45 Val Glu Leu Asp Pro Gly Pro Pro Asp Pro Asp Asp Leu Ala Gln Glu 50 55 60 Met Glu Asp Val Asp Phe Glu Glu Glu Glu Glu Glu Glu Gly Asn Glu 65 70 75 80 Glu Gly Trp Val Leu Glu Pro Gln Glu Gly Val Val Gly Ser Met Glu 85 90 95 Gly Pro Asp Asp Ser Glu Val Thr Phe Ala Leu His Ser Ala Ser Val 100 105 110 Phe Cys Val Ser Leu Asp Pro Lys Thr Asn Thr Leu Ala Val Thr Gly 115 120 125 Gly Glu Asp Asp Lys Ala Phe Val Trp Arg Leu Ser Asp Gly Glu Leu 130 135 140 Leu Phe Glu Cys Ala Gly His Lys Asp Ser Val Thr Cys Ala Gly Phe 145 150 155 160 Ser His Asp Ser Thr Leu Val Ala Thr Gly Asp Met Ser Gly Leu Leu 165 170 175 Lys Val Trp Gln Val Asp Thr Lys Glu Glu Val Trp Ser Phe Glu Ala 180 185 190 Gly Asp Leu Glu Trp Met Glu Trp His Pro Arg Ala Pro Val Leu Leu 195 200 205 Ala Gly Thr Ala Asp Gly Asn Thr Trp Met Trp Lys Val Pro Asn Gly 210 215 220 Asp Cys Lys Thr Phe Gln Gly Pro Asn Cys Pro Ala Thr Cys Gly Arg 225 230 235 240 Val Leu Pro Asp Gly Lys Arg Ala Val Val Gly Tyr Glu Asp Gly Thr 245 250 255 Ile Arg Ile Trp Asp Leu Lys Gln Gly Ser Pro Ile His Val Leu Lys 260 265 270 Gly Thr Glu Gly His Gln Gly Pro Leu Thr Cys Val Ala Ala Asn Gln 275 280 285 Asp Gly Ser Leu Ile Leu Thr Gly Ser Val Asp Cys Gln Ala Lys Leu 290 295 300 Val Ser Ala Thr Thr Gly Lys Val Val Gly Val Phe Arg Pro Glu Thr 305 310 315 320 Val Ala Ser Gln Pro Ser Leu Gly Glu Gly Glu Glu Ser Glu Ser Asn 325 330 335 Ser Val Glu Ser Leu Gly Phe Cys Ser Val Met Pro Leu Ala Ala Val 340 345 350 Gly Tyr Leu Asp Gly Thr Leu Ala Ile Tyr Asp Leu Ala Thr Gln Thr 355 360 365 Leu Arg His Gln Cys Gln His Gln Ser Gly Ile Val Gln Leu Leu Trp 370 375 380 Glu Ala Gly Thr Ala Val Val Tyr Thr Cys Ser Leu Asp Gly Ile Val 385 390 395 400 Arg Leu Trp Asp Ala Arg Thr Gly Arg Leu Leu Thr Asp Tyr Arg Gly 405 410 415 His Thr Ala Glu Ile Leu Asp Phe Ala Leu Ser Lys Asp Ala Ser Leu 420 425 430 Val Val Thr Thr Ser Gly Asp His Lys Ala Lys Val Phe Cys Val Gln 435 440 445 Arg Pro Asp Arg Asp Phe Ser Pro Asp Gly Ala Leu Leu Ala Thr Ala 450 455 460 Ser Tyr Asp Thr Arg Val Tyr Ile Trp Asp Pro His Asn Gly Asp Ile 465 470 475 480 Leu Met Glu Phe Gly His Leu Phe Pro Pro Pro Thr Pro Ile Phe Ala 485 490 495 Gly Gly Ala Asn Asp Arg Trp Val Arg Ser Val Ser Phe Ser His Asp 500 505 510 Gly Leu His Val Ala Ser Leu Ala Asp Asp Lys Met Val Arg Phe Trp 515 520 525 Arg Ile Asp Glu Asp Tyr Pro Val Gln Val Ala Pro Leu Ser Asn Gly 530 535 540 Leu Cys Cys Ala Phe Ser Thr Asp Gly Ser Val Leu Ala Ala Gly Thr 545 550 555 560 His Asp Gly Ser Val Tyr Phe Trp Ala Thr Pro Arg Gln Val Pro Ser 565 570 575 Leu Gln His Leu Cys Arg Met Ser Ile Arg Arg Val Met Pro Thr Gln 580 585 590 Glu Val Gln Glu Leu Pro Ile Pro Ser Lys Leu Leu Glu Phe Leu Ser 595 600 605 Tyr Arg Ile 610 <210> SEQ ID NO 29 <211> LENGTH: 240 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 102 <400> SEQUENCE: 29 Met Ser Ala Pro Thr Met Arg Ser Thr Ser Ile Leu Thr Glu His Leu 1 5 10 15 Gly Tyr Pro Pro Ile Ser Leu Val Asp Asp Ile Ile Asn Ala Val Asn 20 25 30 Glu Ile Met Tyr Lys Cys Thr Ala Ala Met Glu Lys Tyr Leu Leu Ser 35 40 45 Lys Ser Lys Ile Gly Glu Glu Asp Tyr Gly Glu Glu Ile Lys Ser Gly 50 55 60 Val Ala Lys Leu Glu Ser Leu Leu Glu Asn Ser Val Asp Lys Asn Phe 65 70 75 80 Asp Lys Leu Glu Leu Tyr Val Leu Arg Asn Val Leu Arg Ile Pro Glu 85 90 95 Glu Tyr Leu Asp Ala Asn Val Phe Arg Leu Glu Asn Gln Lys Asp Leu 100 105 110 Val Ile Val Asp Glu Asn Glu Leu Lys Lys Ser Glu Glu Lys Leu Arg 115 120 125 Glu Lys Val Asn Asp Val Glu Leu Ala Phe Lys Lys Asn Glu Met Leu 130 135 140 Leu Lys Arg Val Thr Lys Val Lys Arg Leu Leu Phe Thr Ile Arg Gly 145 150 155 160 Phe Lys Gln Lys Leu Asn Glu Leu Leu Lys Cys Lys Asp Asp Val Gln 165 170 175 Leu Gln Lys Ile Leu Glu Ser Leu Lys Pro Ile Asp Asp Thr Met Thr 180 185 190 Leu Leu Thr Asp Ser Leu Arg Lys Leu Tyr Val Asp Ser Glu Ser Thr 195 200 205 Ser Ser Thr Glu Glu Val Glu Ala Leu Leu Gln Arg Leu Lys Thr Asn 210 215 220 Gly Lys Gln Asn Asn Lys Asp Phe Arg Thr Arg Tyr Ile Asp Ile Arg 225 230 235 240 <210> SEQ ID NO 30 <211> LENGTH: 314 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 103 <400> SEQUENCE: 30 Met Ser Asp Lys Thr Leu Asp Glu Arg Thr Thr Ala Ile Leu Thr Glu 1 5 10 15 His Leu Glu Phe Ala Pro Leu Thr Leu Ile Asp Asp Val Ile Asn Ala 20 25 30 Val Asn Glu Ile Met Tyr Lys Gly Thr Thr Ala Ile Glu Thr Tyr Leu 35 40 45 Lys Glu Gln Lys Gln Leu Met Lys Asn Gly Ile Thr Lys Val Thr Glu 50 55 60 Asp Glu Ile Glu Ile Gly Met Gly Lys Leu Glu Ser Leu Leu Glu Ser 65 70 75 80 Thr Ile Asp Lys Asn Phe Asp Lys Phe Glu Leu Tyr Cys Leu Arg Asn 85 90 95 Ile Phe Asn Ile Pro Lys Asp Leu Ile Pro Tyr Ile Gln Leu Ser His 100 105 110 Gln Gln Gly Ile Glu Phe Lys Ser Asp Asn Val Glu Gln Lys Arg Glu 115 120 125 Phe Asp Gln Gln Ile Lys Asn Leu Gln Leu Lys Ile Met Gln Glu Leu 130 135 140 Gln Leu Arg Lys Ile Leu Lys Leu Gln Leu Val Lys Val Gln Lys Leu 145 150 155 160 Ile Lys Val Leu Ile Ala Ile Asp Asn Asp Phe Lys Lys Ile Asp Phe 165 170 175 Ala Ser Gly Gly Gly Gly Asn Glu Glu Ser Ile Arg Ile Leu Lys Asn 180 185 190 Leu Gln Pro Ile Asp Glu Thr Leu Tyr Phe Leu Ile Ser Gln Ile Lys 195 200 205 Asn Leu Ile Asn Gln Ile Glu Gln Leu Ser Asn Lys Val Asn Thr Asn 210 215 220 Leu Lys Thr Gln Lys Phe Ile Pro Asn Leu Arg Asp Lys Phe Ile Asp 225 230 235 240 Gly Arg Thr Phe Arg Val Leu Gln Gln Thr Gly Ile Trp Lys Asp Leu 245 250 255 Glu Lys Asn Asp Ile Lys Ile Leu Val Gln Gly Asn Asp Asn Asn Asn 260 265 270 Asn Asn Asn Asn Asn Asn Asn Asn Thr Leu Thr Asp Leu Gln Asn Gln 275 280 285 Asp Asp Ile Asp Met Ile Ile Pro Glu Gln Asp Asp Ile Asp Val Asp 290 295 300 Ala Ile Lys Asn Ile Asn Ala Gln Ile Phe 305 310 <210> SEQ ID NO 31 <211> LENGTH: 600 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 104 <400> SEQUENCE: 31 Met Ser His Ser Gly Ala Ala Ile Phe Glu Lys Val Ser Gly Ile Ile 1 5 10 15 Ala Ile Asn Glu Asp Val Ser Pro Ala Glu Leu Thr Trp Arg Ser Thr 20 25 30 Asp Gly Asp Lys Val His Thr Val Val Leu Ser Thr Ile Asp Lys Leu 35 40 45 Gln Ala Thr Pro Ala Ser Ser Glu Lys Met Met Leu Arg Leu Ile Gly 50 55 60 Lys Val Asp Glu Ser Lys Lys Arg Lys Asp Asn Glu Gly Asn Glu Val 65 70 75 80 Val Pro Lys Pro Gln Arg His Met Phe Ser Phe Asn Asn Arg Thr Val 85 90 95 Met Asp Asn Ile Lys Met Thr Leu Gln Gln Ile Ile Ser Arg Tyr Lys 100 105 110 Asp Ala Asp Ile Tyr Glu Glu Lys Arg Arg Arg Glu Glu Ser Ala Gln 115 120 125 His Thr Glu Thr Pro Met Ser Ser Ser Ser Val Thr Ala Gly Thr Pro 130 135 140 Thr Pro His Leu Asp Thr Pro Gln Leu Asn Asn Gly Ala Pro Leu Ile 145 150 155 160 Asn Thr Ala Lys Leu Asp Asp Ser Leu Ser Lys Glu Lys Leu Leu Thr 165 170 175 Asn Leu Lys Leu Gln Gln Ser Leu Leu Lys Gly Asn Lys Val Leu Met 180 185 190 Lys Val Phe Gln Glu Thr Val Ile Asn Ala Gly Leu Pro Pro Ser Glu 195 200 205 Phe Trp Ser Thr Arg Ile Pro Leu Leu Arg Ala Phe Ala Leu Ser Thr 210 215 220 Ser Gln Lys Val Gly Pro Tyr Asn Val Leu Ser Thr Ile Lys Pro Val 225 230 235 240 Ala Ser Ser Glu Asn Lys Val Asn Val Asn Leu Ser Arg Glu Lys Ile 245 250 255 Leu Asn Ile Phe Glu Asn Tyr Pro Ile Val Lys Lys Ala Tyr Thr Asp 260 265 270 Asn Val Pro Lys Asn Phe Lys Glu Pro Glu Phe Trp Ala Arg Phe Phe 275 280 285 Ser Ser Lys Leu Phe Arg Lys Leu Arg Gly Glu Lys Ile Met Gln Asn 290 295 300 Asp Arg Gly Asp Val Ile Ile Asp Arg Tyr Leu Thr Leu Asp Gln Glu 305 310 315 320 Phe Asp Arg Lys Asp Asp Asp Met Leu Leu His Pro Val Lys Lys Ile 325 330 335 Ile Asp Leu Asp Gly Asn Ile Gln Asp Asp Pro Val Val Arg Gly Asn 340 345 350 Arg Pro Asp Phe Thr Met Gln Pro Gly Val Asp Ile Asn Gly Asn Ser 355 360 365 Asp Gly Thr Val Asp Ile Leu Lys Gly Met Asn Arg Leu Ser Glu Lys 370 375 380 Met Ile Met Ala Leu Lys Asn Glu Tyr Ser Arg Thr Asn Leu Gln Asn 385 390 395 400 Lys Ser Asn Ile Thr Asn Asp Glu Glu Asp Glu Asp Asn Asp Glu Arg 405 410 415 Asn Glu Leu Lys Ile Asp Asp Leu Asn Glu Ser Tyr Lys Thr Asn Tyr 420 425 430 Ala Ile Ile His Leu Lys Arg Asn Ala His Glu Lys Thr Thr Asp Asn 435 440 445 Asp Ala Lys Ser Ser Ala Asp Ser Ile Lys Asn Ala Asp Leu Lys Val 450 455 460 Ser Asn Gln Gln Met Leu Gln Gln Leu Ser Leu Val Met Asp Asn Leu 465 470 475 480 Ile Asn Lys Leu Asp Leu Asn Gln Val Val Pro Asn Asn Glu Val Ser 485 490 495 Asn Lys Ile Asn Lys Arg Val Ile Thr Ala Ile Lys Ile Asn Ala Lys 500 505 510 Gln Ala Lys His Asn Asn Val Asn Ser Ala Leu Gly Ser Phe Val Asp 515 520 525 Asn Thr Ser Gln Ala Asn Glu Leu Glu Val Lys Ser Thr Leu Pro Ile 530 535 540 Asp Leu Leu Glu Ser Cys Arg Met Leu His Thr Thr Cys Cys Glu Phe 545 550 555 560 Leu Lys His Phe Tyr Ile His Phe Gln Ser Gly Glu Gln Lys Gln Ala 565 570 575 Ser Thr Val Lys Lys Leu Tyr Asn His Leu Lys Asp Cys Ile Glu Lys 580 585 590 Leu Asn Glu Leu Phe Gln Asp Val 595 600 <210> SEQ ID NO 32 <211> LENGTH: 670 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 105 <400> SEQUENCE: 32 Met Asp Ile Ile Arg Gly Ala Cys Ser Val Asp Lys Ile Gly Gly Met 1 5 10 15 Val Tyr Ile Arg Glu Asp Leu Ala Pro Leu Met Leu Glu Trp Lys Pro 20 25 30 Ile Asp Glu Gln Glu Glu Asp Arg Ala Ile Ser Ile Pro Leu Asn Ser 35 40 45 Leu Thr Thr Leu Gln Ser Thr Lys Glu Thr Ser Pro Lys Met Ile Leu 50 55 60 Lys Ile Val Tyr Lys Leu Thr Ser Gly Pro Pro Asn Thr Asn Ala Asp 65 70 75 80 Gly Thr Asp Asn Gly Gly Gly Gly Gly Gly Glu Gln Lys Ser Phe Lys 85 90 95 Leu Thr Phe Thr Asn Arg Pro Thr Met Asn Thr Ile Lys Asp Ser Leu 100 105 110 Gln Thr Ile Val Ala Arg Ser Arg Thr Lys Gly Gly Leu Lys Val Pro 115 120 125 Val Leu Gln Leu Gln Leu Gln His Gln Leu Gln His Leu Gly Ser Ala 130 135 140 Pro Gln Ala Asp Ser Thr Arg Asp Ser Thr Ser Ser Ser Thr Pro Ile 145 150 155 160 Pro Pro Thr Thr Ser Gly Thr Ser Thr Ser Ser Ser Leu Leu Ser Leu 165 170 175 Ala Ala Ser Gln Ser Leu Ser Asp Ala Asn Leu Leu Lys Asn Phe Glu 180 185 190 Leu Gln Gln Lys Leu Leu Leu Glu Asp Arg Gln Leu Arg Asp Val Phe 195 200 205 Thr Lys Ser Val Met Gln Phe Lys Leu Ser Pro Gln Val Phe Trp Ser 210 215 220 Ser Arg Leu Asn Gln Leu Arg Thr Phe Ala Leu Thr Ile Ser Gln His 225 230 235 240 Lys Gly Pro Tyr Asn Val Leu Ser Thr Ile Lys Pro Val Ala Thr Ser 245 250 255 Asp Asn Gln Val Asn Val Asn Val Thr Arg Asp Thr Ile Asn Glu Ile 260 265 270 Phe Thr Ile Tyr Pro Ile Ile Lys Lys Ala Phe Asp Asp Leu Val Pro 275 280 285 Asn Lys Phe Asn Glu Gly Glu Phe Trp Ser Arg Phe Phe Asn Ser Lys 290 295 300 Leu Phe Arg Arg Leu Arg Gly Asp Lys Ile Ser Ile Ser Asn Ser Arg 305 310 315 320 Gly Asp Val Val Leu Asp Lys Tyr Leu Tyr Ile Asp Gln Asn Tyr Gln 325 330 335 Glu Lys Leu Gln Lys Ser Ser Thr Leu Glu Asn Asn Gly Ser Gly Gly 340 345 350 Gly Gly Gly Gly Ala Gly Gly Gly Ser Gly Asn Ser Glu Gln Gly Ile 355 360 365 Gln Thr Leu Glu Ser Pro His Val Lys Lys Phe Leu Asp Leu Met Gly 370 375 380 Asn Gln Gln Asp Asn Ser Gln Lys Leu Gly Asn Arg Pro Asp Phe Thr 385 390 395 400 Met Arg Tyr Asp Glu Asp Asn Val Asp Asp Asp Asn Lys Lys Pro Thr 405 410 415 Leu Gly Asn Glu Asn Glu Met Ile Ile Leu Met Lys Asn Met Asn Arg 420 425 430 Leu Ser Ser Lys Met Met Ser Met Ser Ser Thr Asn Gly Pro Glu Lys 435 440 445 Pro Ser Glu Thr Thr Ile Asp Gly Leu Ser Ala Ala Glu Leu Asn Glu 450 455 460 Tyr Glu Glu Glu Leu Asp Leu His Asp Leu Asn Asp Ser Glu Asn Leu 465 470 475 480 Gln Tyr Ile Lys Leu Asn Ile Asn Thr Asp Ile Ala Lys Gly Thr Lys 485 490 495 Leu Asp Ser Tyr Glu Gly Ser Asn Thr Asn Asn Lys Ile Ser Gln Asp 500 505 510 Glu Leu His Lys Tyr Leu Gln Ser Gln Thr Phe Gln Gly Gln Ile Glu 515 520 525 Leu Thr Glu Thr Tyr Thr Cys Lys Ser Glu Glu Ile Glu Lys Thr Ser 530 535 540 Met Glu Ile Ala Met Leu Ile Lys Gln Asn Phe Arg Thr Phe Lys Leu 545 550 555 560 Ile Asn Lys Glu Asn Asp Ile Ala Gly Thr Asn Ile Val Pro Asn Ser 565 570 575 Leu Ile Gln Glu Ile Ile Thr Tyr Asn Ile Thr Ile Val Glu Phe Leu 580 585 590 Ser His Phe Trp Lys Ile Phe Leu His Gly Asn Asn Pro Gly Gln Leu 595 600 605 Lys Lys Ile Phe Thr Ser Leu Lys Asn Cys Gln Ser Gly Leu Ile Glu 610 615 620 Leu Glu Asn Lys Ala Ile Asp Gln Phe Lys Ser Met Asp Ile Leu Gln 625 630 635 640 Lys Asn Gln Lys Leu Gln Asp Lys Val Leu Lys Asp Phe Ala Ser Cys 645 650 655 Leu Gln Pro Met Lys Ile Ala Leu Asp Lys Ala Cys Asn Glu 660 665 670 <210> SEQ ID NO 33 <211> LENGTH: 498 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 106 <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/W19128 <309> DATABASE ENTRY DATE: 1996-05-03 <313> RELEVANT RESIDUES: (1)..(498) <400> SEQUENCE: 33 Met Ala Thr Ser Ser Glu Glu Val Leu Leu Ile Val Lys Lys Val Arg 1 5 10 15 Gln Lys Lys Gln Asp Gly Ala Leu Tyr Leu Met Ala Glu Arg Ile Ala 20 25 30 Trp Ala Pro Glu Gly Lys Asp Arg Phe Thr Ile Ser His Met Tyr Ala 35 40 45 Asp Ile Lys Cys Gln Lys Ile Ser Pro Glu Gly Lys Ala Lys Ile Gln 50 55 60 Leu Gln Leu Val Leu His Ala Gly Asp Thr Thr Asn Phe His Phe Ser 65 70 75 80 Asn Glu Ser Thr Ala Val Lys Glu Arg Asp Ala Val Lys Asp Leu Leu 85 90 95 Gln Gln Leu Leu Pro Phe Lys Arg Ala Asn Lys Glu Leu Glu Lys Asn 100 105 110 Arg Cys Cys Lys Ile Leu Phe Cys Phe Ser Phe Ile Lys Leu Arg Thr 115 120 125 Gly Glu Glu Gln Met Leu Glu Asp Pro Val Leu Phe Gln Leu Tyr Lys 130 135 140 Asp Val Ser Gln Val Ile Ser Ala Glu Glu Phe Trp Asn Arg Leu Asn 145 150 155 160 Val Asn Ala Thr Asp Ser Ser Thr Ser Asn His Lys Gln Asp Val Gly 165 170 175 Ile Ser Ala Ala Phe Leu Ala Asp Val Arg Pro Gln Thr Asp Gly Cys 180 185 190 Asn Gly Leu Arg Tyr Asn Leu Thr Ser Asp Ile Ile Glu Ser Ile Phe 195 200 205 Arg Thr Tyr Pro Ala Val Lys Met Lys Tyr Ala Glu Asn Val Pro His 210 215 220 Asn Met Thr Glu Lys Glu Phe Trp Thr Arg Phe Phe Gln Ser His Tyr 225 230 235 240 Phe His Arg Asp Arg Leu Asn Thr Gly Ser Lys Asp Leu Phe Ala Glu 245 250 255 Cys Ala Lys Ile Asp Glu Lys Gly Leu Lys Thr Met Val Ser Leu Gly 260 265 270 Val Lys Asn Pro Leu Leu Asp Leu Thr Ala Leu Glu Asp Lys Pro Leu 275 280 285 Asp Glu Gly Tyr Gly Ile Ser Ser Val Pro Ser Ser Asn Ser Lys Ser 290 295 300 Ile Lys Glu Asn Ser Asn Ala Ala Ile Ile Lys Arg Phe Asn His His 305 310 315 320 Ser Ala Met Val Leu Ala Ala Gly Leu Arg Lys Gln Glu Ala Gln Asn 325 330 335 Glu Gln Thr Ser Glu Pro Ser Asn Met Asp Gly Asn Ser Gly Asp Ala 340 345 350 Asp Cys Phe Gln Pro Ala Val Lys Arg Ala Lys Leu Gln Glu Ser Ile 355 360 365 Glu Tyr Glu Asp Leu Gly Lys Asn Asn Ser Val Lys Thr Ile Ala Leu 370 375 380 Asn Leu Lys Lys Ser Asp Arg Tyr Tyr His Gly Pro Thr Pro Ile Gln 385 390 395 400 Ser Leu Gln Tyr Ala Thr Ser Gln Asp Ile Ile Asn Ser Phe Gln Ser 405 410 415 Ile Arg Gln Glu Met Glu Ala Tyr Thr Pro Lys Leu Thr Gln Val Leu 420 425 430 Ser Ser Ser Ala Ala Ser Ser Thr Ile Thr Ala Leu Ser Pro Gly Gly 435 440 445 Ala Leu Met Gln Gly Gly Thr Gln Gln Ala Ile Asn Gln Met Val Pro 450 455 460 Asn Asp Ile Gln Thr Asn Leu Val Ser His Ile Glu Glu Met Leu Gln 465 470 475 480 Thr Ala Tyr Asn Lys Leu His Thr Trp Gln Ser Arg Arg Leu Met Lys 485 490 495 Lys Thr <210> SEQ ID NO 34 <211> LENGTH: 846 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 107 <400> SEQUENCE: 34 Met Glu Leu Glu Pro Thr Leu Phe Gly Ile Ile Glu Ala Leu Ala Pro 1 5 10 15 Gln Leu Leu Ser Gln Ser His Leu Gln Thr Phe Val Ser Asp Val Val 20 25 30 Asn Leu Leu Arg Ser Ser Thr Lys Ser Ala Thr Gln Leu Gly Pro Leu 35 40 45 Ile Asp Phe Tyr Lys Leu Gln Ser Leu Asp Ser Pro Glu Thr Thr Ile 50 55 60 Met Trp His Lys Ile Glu Lys Phe Leu Asp Ala Leu Phe Gly Ile Gln 65 70 75 80 Asn Thr Asp Asp Met Val Lys Tyr Leu Ser Val Phe Gln Ser Leu Leu 85 90 95 Pro Ser Asn Tyr Arg Ala Lys Ile Val Gln Lys Ser Ser Gly Leu Asn 100 105 110 Met Glu Asn Leu Ala Asn His Glu His Leu Leu Ser Pro Val Arg Ala 115 120 125 Pro Ser Ile Tyr Thr Glu Ala Ser Phe Glu Asn Met Asp Arg Phe Ser 130 135 140 Glu Arg Arg Ser Met Val Ser Ser Pro Asn Arg Tyr Val Pro Ser Ser 145 150 155 160 Thr Tyr Ser Ser Val Thr Leu Arg Gln Leu Ser Asn Pro Tyr Tyr Val 165 170 175 Asn Thr Ile Pro Glu Glu Asp Ile Leu Lys Tyr Val Ser Tyr Thr Leu 180 185 190 Leu Ala Thr Thr Ser Ala Leu Phe Pro Phe Asp His Glu Gln Ile Gln 195 200 205 Ile Pro Ser Lys Ile Pro Asn Phe Glu Ser Gly Leu Leu His Leu Ile 210 215 220 Phe Glu Ala Gly Leu Leu Tyr Gln Ser Leu Gly Tyr Lys Val Glu Lys 225 230 235 240 Phe Arg Met Leu Asn Ile Ser Pro Met Lys Lys Ala Leu Ile Ile Glu 245 250 255 Ile Ser Glu Glu Leu Gln Asn Tyr Thr Ala Phe Val Asn Asn Leu Val 260 265 270 Ser Ser Gly Thr Val Val Ser Leu Lys Ser Leu Tyr Arg Glu Ile Tyr 275 280 285 Glu Asn Ile Ile Arg Leu Arg Ile Tyr Cys Arg Phe Thr Glu His Leu 290 295 300 Glu Glu Leu Ser Gly Asp Thr Phe Leu Ile Glu Leu Asn Ile Phe Lys 305 310 315 320 Ser His Gly Asp Leu Thr Ile Arg Lys Ile Ala Thr Asn Leu Phe Asn 325 330 335 Ser Met Ile Ser Leu Tyr Tyr Glu Tyr Leu Met Asn Trp Leu Thr Lys 340 345 350 Gly Leu Leu Arg Ala Thr Tyr Gly Glu Phe Phe Ile Ala Glu Asn Thr 355 360 365 Asp Thr Asn Gly Thr Asp Asp Asp Phe Ile Tyr His Ile Pro Ile Glu 370 375 380 Phe Asn Gln Glu Arg Val Pro Ala Phe Ile Pro Lys Glu Leu Ala Tyr 385 390 395 400 Lys Ile Phe Met Ile Gly Lys Ser Tyr Ile Phe Leu Glu Lys Tyr Cys 405 410 415 Lys Glu Val Gln Trp Thr Asn Glu Phe Ser Lys Lys Tyr His Val Leu 420 425 430 Tyr Gln Ser Asn Ser Tyr Arg Gly Ile Ser Thr Asn Phe Phe Glu Ile 435 440 445 Ile Asn Asp Gln Tyr Ser Glu Ile Val Asn His Thr Asn Gln Ile Leu 450 455 460 Asn Gln Lys Phe His Tyr Arg Asp Val Val Phe Ala Leu Lys Asn Ile 465 470 475 480 Leu Leu Met Gly Lys Ser Asp Phe Met Asp Ala Leu Ile Glu Lys Ala 485 490 495 Asn Asp Ile Leu Ala Thr Pro Ser Asp Ser Leu Pro Asn Tyr Lys Leu 500 505 510 Thr Arg Val Leu Gln Glu Ala Val Gln Leu Ser Ser Leu Arg His Leu 515 520 525 Met Asn Ser Pro Arg Asn Ser Ser Val Ile Asn Gly Leu Asp Ala Arg 530 535 540 Val Leu Asp Leu Gly His Gly Ser Val Gly Trp Asp Val Phe Thr Leu 545 550 555 560 Asp Tyr Ile Leu Tyr Pro Pro Leu Ser Leu Val Leu Asn Val Asn Arg 565 570 575 Pro Phe Gly Arg Lys Glu Tyr Leu Arg Ile Phe Asn Phe Leu Trp Arg 580 585 590 Phe Lys Lys Asn Asn Tyr Phe Tyr Gln Lys Glu Met Leu Lys Ser Asn 595 600 605 Asp Ile Ile Arg Ser Phe Lys Lys Ile Arg Gly Tyr Asn Pro Leu Ile 610 615 620 Arg Asp Ile Ile Asn Lys Leu Ser Arg Ile Ser Ile Leu Arg Thr Gln 625 630 635 640 Phe Gln Gln Phe Asn Ser Lys Met Glu Ser Tyr Tyr Leu Asn Cys Ile 645 650 655 Ile Glu Glu Asn Phe Lys Glu Met Thr Arg Lys Leu Gln Arg Thr Glu 660 665 670 Asn Lys Ser Gln Asn Gln Phe Asp Leu Ile Arg Leu Asn Asn Gly Thr 675 680 685 Ile Glu Leu Asn Gly Ile Leu Thr Pro Lys Ala Glu Val Leu Thr Lys 690 695 700 Ser Ser Ser Ser Lys Pro Gln Lys His Ala Ile Glu Lys Thr Leu Asn 705 710 715 720 Ile Asp Glu Leu Glu Ser Val His Asn Thr Phe Leu Thr Asn Ile Leu 725 730 735 Ser His Lys Leu Phe Ala Thr Asn Thr Ser Glu Ile Ser Val Gly Asp 740 745 750 Tyr Ser Gly Gln Pro Tyr Pro Thr Ser Leu Val Leu Leu Leu Asn Ser 755 760 765 Val Tyr Glu Phe Val Lys Val Tyr Cys Asn Leu Asn Asp Ile Gly Tyr 770 775 780 Glu Ile Phe Ile Lys Met Asn Leu Asn Asp His Glu Ala Ser Asn Gly 785 790 795 800 Leu Leu Gly Lys Phe Asn Thr Asn Leu Lys Glu Ile Val Ser Gln Tyr 805 810 815 Lys Asn Phe Lys Asp Arg Leu Tyr Ile Phe Arg Ala Asp Leu Lys Asn 820 825 830 Asp Gly Asp Glu Glu Leu Phe Leu Leu Ser Lys Ser Leu Arg 835 840 845 <210> SEQ ID NO 35 <211> LENGTH: 712 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 108 <400> SEQUENCE: 35 Met Ala Leu Asn Lys Val Gln Leu Ile Lys Leu Tyr Ser Asn Arg Leu 1 5 10 15 Val Lys Ser Leu Val Pro Val Glu Phe Gly Glu Ala Phe Ile Gln Ser 20 25 30 Ile Ile Asn Asp Leu Gln Thr Thr Leu Leu Asn Thr Ser Ser Glu Glu 35 40 45 Gln Asn Leu Ser Ile Ile Ile Asn Lys Leu Lys Met Gln Phe Leu Ser 50 55 60 Asn Asn Leu Lys Asn Glu Trp Val Glu Phe Gln Asn Ile Val Asn Ser 65 70 75 80 Leu Ser Lys Phe Lys Ser Leu Asp Gln Ile Cys Asn Tyr Leu Ala Phe 85 90 95 Leu Asp Ala Leu Arg Asp Glu Lys Pro Glu Asp Ile Leu Ser Thr Ser 100 105 110 Thr Ala Ser Leu Ser Pro Gly Lys Gln Asn Val Met Ile Asn Thr Val 115 120 125 Asn Thr Ala Leu Thr Leu Ser Gln Leu Ile Glu Pro Tyr Tyr Asp Thr 130 135 140 Leu Ser Glu Gln Thr Ile Leu Thr Tyr Leu Pro Tyr Thr Met Leu Gly 145 150 155 160 Leu Asp Ser Lys Ile Phe Thr Phe Ser Asn Asn Tyr Thr Arg Leu Glu 165 170 175 Ile Pro Lys Asp Ile Asn Asn Ser Phe Ser Ser Leu Leu Arg Glu Val 180 185 190 Phe Glu Phe Ala Ile Leu Tyr Lys Gln Leu Ala Ile Val Val Asp Arg 195 200 205 Tyr Lys Gly Thr Leu Val Leu Ala Ile Lys Thr Ala Tyr Ile Ala Ile 210 215 220 Leu Glu Ala Gln Leu Asn Lys Tyr Val Asn Asp Ile Asn Asn Ile Phe 225 230 235 240 Asn Asn Lys Pro Asn Ser Ile Leu Val Val Tyr Asn Ser Ile Phe Pro 245 250 255 Trp Ile Ser Ile Leu Arg Phe Leu Tyr Arg Val Ser Asn Arg Leu Asn 260 265 270 Arg Leu Asp Gly Tyr Glu Phe Leu Thr Phe Ile Tyr Ser Phe Thr Asn 275 280 285 His Gly Asp Pro Lys Ile Arg Gly Ile Ala Val Thr Ala Phe Thr Glu 290 295 300 Val Val Lys Pro Tyr Tyr Asn Ile Val Glu His Trp Ile Val Lys Gly 305 310 315 320 Glu Leu Ile Asp Asn Asn Asn Glu Phe Phe Ile Ile Phe Asp Gln Glu 325 330 335 Gln Asn Glu Phe Asn Ser Ile Ile Lys Leu Leu Pro Lys Lys Ile Pro 340 345 350 Ala Phe Ile Lys Ser Ser Asp Lys Ile Phe Gln Ile Gly Thr Thr Leu 355 360 365 Ile Phe Leu Asn Lys Tyr Cys Arg Glu Leu Lys Trp Val Asn Gln Tyr 370 375 380 Asn Val Lys Tyr Ser Ala Ile Leu Phe Asn Asn His Gln Gly Leu Ala 385 390 395 400 Ser Met Thr Thr Asn Glu Met Ile Lys Leu Ile Asp Leu Gln Tyr Asn 405 410 415 Glu Ile Leu Thr Phe Leu Thr Gln Ile Ile Gln Gly Asn Asn Lys Leu 420 425 430 Leu Thr His Val Tyr Asn Ile Lys Arg Tyr Tyr Phe Met Glu Thr Asn 435 440 445 Asp Phe Ile Asp Ala Ile Met Val Lys Gly Lys Asp Val Phe Asn Glu 450 455 460 Ser Ser Val Asn Ile Ser Ser Thr Tyr Leu Arg Lys Val Leu Gln Asp 465 470 475 480 Ala Ile Gln Ile Ser Ser Val Lys Asn Phe Glu Tyr Val Asp Arg Leu 485 490 495 Asp Ser Arg Val Leu Asn Pro Gln His Gly Asn Leu Gly Trp Glu Ser 500 505 510 Phe Thr Ile Glu Tyr Lys Ile Asp Asp Leu Pro Met Ser Tyr Leu Phe 515 520 525 Glu Gly His Gln His Leu Gln Tyr Leu Lys Met Phe His Phe Leu Trp 530 535 540 Lys Leu Arg Gln Leu Asn Asn Leu Leu Asn Trp His Phe Glu Met Phe 545 550 555 560 Asn Glu Leu Asn His Asn Val Val Thr Lys Leu Ser Ser Arg Asn Arg 565 570 575 Arg Pro Leu Ala Lys Ser Leu Ser Ile Ile Thr Ser Ile Arg Phe His 580 585 590 Phe Thr Gln Phe Leu Asn Glu Leu Ile Ala Tyr Leu Ser Tyr Asp Val 595 600 605 Ile Glu Glu Asn Phe Gln Gln His Ile Val Arg Lys Leu Phe Tyr Asn 610 615 620 Lys Asn Asp Gln Asp Leu Leu Leu Asn Lys Leu Phe Met Asn Leu Leu 625 630 635 640 Glu Ile Asp Pro Asn Asn Asp Leu Pro Lys Phe Asn Val Asn Leu Leu 645 650 655 Thr Ile Asp Glu Leu Val Glu Leu His Gly Thr Tyr Ile Asp Ser Ile 660 665 670 Ile Asn Ser Ser Leu Leu Asn Glu Lys Leu Lys Gly Asn Glu Thr Asn 675 680 685 Ile Ser Tyr Ile Asp Gln Ile Phe Asp Ile Leu Gln Thr Ile Phe Asn 690 695 700 Phe Ile Ile Gln Val Arg Asn Ser 705 710 <210> SEQ ID NO 36 <211> LENGTH: 880 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 109 <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/AAC39727 <309> DATABASE ENTRY DATE: 1998-05-06 <313> RELEVANT RESIDUES: (1)..(880) <400> SEQUENCE: 36 Met Ala Thr Pro Asp Gln Lys Ser Pro Asn Val Leu Leu Gln Asn Leu 1 5 10 15 Cys Cys Arg Ile Leu Gly Arg Ser Glu Ala Asp Val Ala Gln Gln Phe 20 25 30 Gln Tyr Ala Val Arg Val Ile Gly Ser Asn Phe Ala Pro Thr Val Glu 35 40 45 Arg Asp Glu Phe Leu Val Ala Glu Lys Ile Lys Lys Glu Leu Ile Arg 50 55 60 Gln Arg Arg Glu Ala Asp Ala Ala Leu Phe Ser Glu Leu His Arg Lys 65 70 75 80 Leu His Ser Gln Gly Val Leu Lys Asn Lys Trp Ser Ile Leu Tyr Leu 85 90 95 Leu Leu Ser Leu Ser Glu Asp Pro Arg Arg Gln Pro Ser Lys Val Ser 100 105 110 Ser Tyr Ala Thr Leu Phe Ala Gln Ala Leu Pro Arg Asp Ala His Ser 115 120 125 Thr Pro Tyr Tyr Tyr Ala Arg Pro Gln Thr Leu Pro Leu Ser Tyr Gln 130 135 140 Asp Arg Ser Ala Gln Ser Ala Gln Ser Ser Gly Ser Val Gly Ser Ser 145 150 155 160 Gly Ile Ser Ser Ile Gly Leu Cys Ala Leu Ser Gly Pro Ala Pro Ala 165 170 175 Pro Gln Ser Leu Leu Pro Gly Gln Ser Asn Gln Ala Pro Gly Val Gly 180 185 190 Asp Cys Leu Arg Gln Gln Leu Gly Ser Arg Leu Ala Trp Thr Leu Thr 195 200 205 Ala Asn Gln Pro Ser Ser Gln Ala Thr Thr Ser Lys Gly Val Pro Ser 210 215 220 Ala Val Ser Arg Asn Met Thr Arg Ser Arg Arg Glu Gly Asp Thr Gly 225 230 235 240 Gly Thr Met Glu Ile Thr Glu Ala Ala Leu Val Arg Asp Ile Leu Tyr 245 250 255 Val Phe Gln Gly Ile Asp Gly Lys Asn Ile Lys Met Asn Asn Thr Glu 260 265 270 Asn Cys Tyr Lys Val Glu Gly Lys Ala Asn Leu Ser Arg Ser Leu Arg 275 280 285 Asp Thr Ala Val Arg Leu Ser Glu Leu Gly Trp Leu His Asn Lys Ile 290 295 300 Arg Arg Tyr Thr Asp Gln Arg Ser Leu Asp Arg Ser Phe Gly Leu Val 305 310 315 320 Gly Gln Ser Phe Cys Ala Ala Leu His Gln Glu Leu Arg Glu Tyr Tyr 325 330 335 Arg Leu Leu Ser Val Leu His Ser Gln Leu Gln Leu Glu Asp Asp Gln 340 345 350 Gly Val Asn Leu Gly Leu Glu Ser Ser Leu Thr Leu Arg Arg Leu Leu 355 360 365 Val Trp Thr Tyr Asp Pro Lys Ile Arg Leu Lys Thr Leu Ala Ala Leu 370 375 380 Val Asp His Cys Gln Gly Arg Lys Gly Gly Glu Leu Ala Ser Ala Val 385 390 395 400 His Ala Tyr Thr Lys Thr Gly Asp Pro Tyr Met Arg Ser Leu Val Gln 405 410 415 His Ile Leu Ser Leu Val Ser His Pro Val Leu Ser Phe Leu Tyr Arg 420 425 430 Trp Ile Tyr Asp Gly Glu Leu Glu Asp Thr Tyr His Glu Phe Phe Val 435 440 445 Ala Ser Asp Pro Thr Val Lys Thr Asp Arg Leu Trp His Asp Lys Tyr 450 455 460 Thr Leu Arg Lys Ser Met Ile Pro Ser Phe Met Thr Met Asp Gln Ser 465 470 475 480 Arg Lys Val Leu Leu Ile Gly Lys Ser Ile Asn Phe Leu His Gln Val 485 490 495 Cys His Asp Gln Thr Pro Thr Thr Lys Met Ile Ala Val Thr Lys Ser 500 505 510 Ala Glu Ser Pro Gln Asp Ala Ala Asp Leu Phe Thr Asp Leu Glu Asn 515 520 525 Ala Phe Gln Gly Lys Ile Asp Ala Ala Tyr Phe Glu Thr Ser Lys Tyr 530 535 540 Leu Leu Asp Val Leu Asn Lys Lys Tyr Ser Leu Leu Asp His Met Gln 545 550 555 560 Ala Met Arg Arg Tyr Leu Leu Leu Gly Gln Gly Asp Phe Ile Arg His 565 570 575 Leu Met Asp Leu Leu Lys Pro Glu Leu Val Arg Pro Ala Thr Thr Leu 580 585 590 Tyr Gln His Asn Leu Thr Gly Ile Leu Glu Thr Ala Val Arg Ala Thr 595 600 605 Asn Ala Gln Phe Asp Ser Pro Glu Ile Leu Arg Arg Leu Asp Val Arg 610 615 620 Leu Leu Glu Val Ser Pro Gly Asp Thr Gly Trp Asp Val Phe Ser Leu 625 630 635 640 Asp Tyr His Val Asp Gly Pro Ile Ala Thr Val Phe Thr Arg Glu Cys 645 650 655 Met Ser His Tyr Leu Arg Val Phe Asn Phe Leu Trp Arg Ala Lys Arg 660 665 670 Met Glu Tyr Ile Leu Thr Asp Ile Arg Lys Gly His Met Cys Asn Ala 675 680 685 Lys Leu Leu Arg Asn Met Pro Glu Phe Ser Gly Val Leu His Gln Cys 690 695 700 His Ile Leu Ala Ser Glu Met Val His Phe Ile His Gln Met Gln Tyr 705 710 715 720 Tyr Ile Thr Phe Glu Val Leu Glu Cys Ser Trp Asp Glu Leu Trp Asn 725 730 735 Lys Val Gln Gln Ala Gln Asp Leu Asp His Ile Ile Ala Ala His Glu 740 745 750 Val Phe Leu Asp Thr Ile Ile Ser Arg Cys Leu Leu Asp Ser Asp Ser 755 760 765 Arg Ala Leu Leu Asn Gln Leu Arg Ala Val Phe Asp Gln Ile Ile Glu 770 775 780 Leu Gln Asn Ala Gln Asp Ala Ile Tyr Arg Ala Ala Leu Glu Glu Leu 785 790 795 800 Gln Arg Arg Leu Gln Phe Glu Glu Lys Lys Lys Gln Arg Glu Ile Glu 805 810 815 Gly Gln Trp Gly Val Thr Ala Ala Glu Glu Glu Glu Glu Asn Lys Arg 820 825 830 Ile Gly Glu Phe Lys Glu Ser Ile Pro Lys Met Cys Ser Gln Leu Arg 835 840 845 Ile Leu Thr His Phe Tyr Gln Gly Ile Val Gln Gln Phe Leu Val Leu 850 855 860 Leu Thr Thr Ser Ser Asp Glu Ser Leu Arg Phe Leu Ser Phe Arg Leu 865 870 875 880 <210> SEQ ID NO 37 <211> LENGTH: 534 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 110 <400> SEQUENCE: 37 Met Glu Lys Ser Leu Ala Asp Gln Ile Ser Asp Ile Ala Ile Lys Pro 1 5 10 15 Val Asn Lys Asp Phe Asp Ile Glu Asp Glu Glu Asn Ala Ser Leu Phe 20 25 30 Gln His Asn Glu Lys Asn Gly Glu Ser Asp Leu Ser Asp Tyr Gly Asn 35 40 45 Ser Asn Thr Glu Glu Thr Lys Lys Ala His Tyr Leu Glu Val Glu Lys 50 55 60 Ser Lys Leu Arg Ala Glu Lys Gly Leu Glu Leu Asn Asp Pro Lys Tyr 65 70 75 80 Thr Gly Val Lys Gly Ser Arg Gln Ala Leu Tyr Glu Glu Val Ser Glu 85 90 95 Asn Glu Asp Glu Glu Glu Glu Glu Glu Glu Glu Glu Glu Lys Glu Glu 100 105 110 Asp Ala Leu Ser Phe Arg Thr Asp Ser Glu Asp Glu Glu Val Glu Ile 115 120 125 Asp Glu Glu Glu Ser Asp Ala Asp Gly Gly Glu Thr Glu Glu Ala Gln 130 135 140 Gln Lys Arg His Ala Leu Ser Lys Leu Ile Gln Gln Glu Thr Lys Gln 145 150 155 160 Ala Ile Asn Lys Leu Ser Gln Ser Val Gln Arg Asp Ala Ser Lys Gly 165 170 175 Tyr Ser Ile Leu Gln Gln Thr Lys Leu Phe Asp Asn Ile Ile Asp Leu 180 185 190 Arg Ile Lys Leu Gln Lys Ala Val Ile Ala Ala Asn Lys Leu Pro Leu 195 200 205 Thr Thr Glu Ser Trp Glu Glu Ala Lys Met Asp Asp Ser Glu Glu Thr 210 215 220 Lys Arg Leu Leu Lys Glu Asn Glu Lys Leu Phe Asn Asn Leu Phe Asn 225 230 235 240 Arg Leu Ile Asn Phe Arg Ile Lys Phe Gln Leu Gly Asp His Ile Thr 245 250 255 Gln Asn Glu Glu Val Ala Lys His Lys Leu Ser Lys Lys Arg Ser Leu 260 265 270 Lys Glu Leu Tyr Gln Glu Thr Asn Ser Leu Asp Ser Glu Leu Lys Glu 275 280 285 Tyr Arg Thr Ala Val Leu Asn Lys Trp Ser Thr Lys Val Ser Ser Ala 290 295 300 Ser Gly Asn Ala Ala Leu Ser Ser Asn Lys Phe Lys Ala Ile Asn Leu 305 310 315 320 Pro Ala Asp Val Gln Val Glu Asn Gln Leu Ser Asp Met Ser Arg Leu 325 330 335 Met Lys Arg Thr Lys Leu Asn Arg Arg Asn Ile Thr Pro Leu Tyr Phe 340 345 350 Gln Lys Asp Cys Ala Asn Gly Arg Leu Pro Glu Leu Ile Ser Pro Val 355 360 365 Val Lys Asp Ser Val Asp Asp Asn Glu Asn Ser Asp Asp Gly Leu Asp 370 375 380 Ile Pro Lys Asn Tyr Asp Pro Arg Arg Lys Asp Asn Asn Ala Ile Asp 385 390 395 400 Ile Thr Glu Asn Pro Tyr Val Phe Asp Asp Glu Asp Phe Tyr Arg Val 405 410 415 Leu Leu Asn Asp Leu Ile Asp Lys Lys Ile Ser Asn Ala His Asn Ser 420 425 430 Glu Ser Ala Ala Ile Thr Ile Thr Ser Thr Asn Ala Arg Ser Asn Asn 435 440 445 Lys Leu Lys Lys Asn Ile Asp Thr Lys Ala Ser Lys Gly Arg Lys Leu 450 455 460 Asn Tyr Ser Val Gln Asp Pro Ile Ala Asn Tyr Glu Ala Pro Ile Thr 465 470 475 480 Ser Gly Tyr Lys Trp Ser Asp Asp Gln Ile Asp Glu Phe Phe Ala Gly 485 490 495 Leu Leu Gly Gln Arg Val Asn Phe Asn Glu Asn Glu Asp Glu Glu Gln 500 505 510 His Ala Arg Ile Glu Asn Asp Glu Glu Leu Glu Ala Val Lys Asn Asp 515 520 525 Asp Ile Gln Ile Phe Gly 530 <210> SEQ ID NO 38 <211> LENGTH: 480 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 111 <400> SEQUENCE: 38 Met Ser Phe Phe Gly Leu His Phe Gln Leu Asn Ser Leu Thr Leu Asn 1 5 10 15 Ile Ser Asn Met Ala Lys Lys Ser Leu Ser Glu Gln Ile Ser Ser Leu 20 25 30 Tyr Thr Pro Lys Thr Asp Tyr Asp Ile Glu Asp His Asp Leu Asp Val 35 40 45 Ser Lys Asp Asn Gly Ile Phe Gln His His Asp Gly Gly Ser Glu Asn 50 55 60 Glu Ser Glu Asp Glu Asp Thr Gly Leu Arg Asn Glu His Tyr Val Glu 65 70 75 80 Ser Ser Lys Ser Lys Leu Arg Gln Gln Asn Glu Gly Val Asn Leu Gly 85 90 95 Glu Lys Tyr Val Gly Asn Val Thr Ser Arg Ser Lys Leu Tyr Asp Asp 100 105 110 Glu Asp Asp Lys Gln Pro Thr Glu Ala Ser Ser Gly Glu Glu Leu Asp 115 120 125 Ala Glu Ser Ala Glu Glu Glu Glu Asp Glu Glu Ser Glu Asp Val Ala 130 135 140 Asp Asp Asp Glu Asp Asp Gln Glu Ser Asp Arg Ser Ser Ser Ser Asp 145 150 155 160 Ala Glu Asn Asp Glu Asp Glu Asn Ile Ser His Lys Arg Glu Leu Leu 165 170 175 Lys Gln Leu Met Ser Lys Glu Arg Ser His Ile Val Asn Arg Leu Ser 180 185 190 Gln Ser Ala Thr Asn Asp Ala Leu Lys Gly Tyr Ser Ile Gln Gln Gln 195 200 205 Asn Lys Thr Phe Glu Lys Ile Ile Asp Val Arg Leu Lys Phe Gln Lys 210 215 220 Ser Val Thr Ser Ser Asn Met Leu Pro Ile Asn Thr Ser Thr Tyr Ser 225 230 235 240 Glu Thr Lys Ser Glu Asp Ser Asp Glu Leu Val Thr Lys Ala Lys Lys 245 250 255 Gln Leu Tyr Ser Leu Leu Asp His Leu Phe Thr Leu Arg Asn Glu Leu 260 265 270 Asp Glu Ser Thr Ser Val Lys Thr Pro Lys Lys Arg Ser Phe Ala Lys 275 280 285 Tyr Ser Glu Val Thr Ser Ala Ala Asp Ala Gln Leu Asn Ser Arg Arg 290 295 300 Asn Gln Ile Leu Thr Lys Trp Ser Ala Lys Val Ala Asn Ser Ser Gly 305 310 315 320 Arg Asn Ala Met Asn Ala Asn Lys Phe Lys Thr Ile Asn Gln Ser Phe 325 330 335 Glu Gln Gln Val Asn Asn Asn Leu Ser Asp Met Asp Arg Leu Ile Lys 340 345 350 Arg Thr Lys Leu Asn Arg Arg Asn Val Thr Pro Ile Gly Tyr Thr Thr 355 360 365 Lys Glu Glu Asp Asp His Glu Asn Gly Asn Lys Asn Lys Ser Ile Asp 370 375 380 Glu Asp Asp Asp Asp Ile Pro Glu Asp Thr Ser Val Arg Lys Lys Thr 385 390 395 400 Gln Gly Leu Glu Asn Asp Tyr Ile Phe Asp Asp Glu Asp Phe Tyr Arg 405 410 415 Val Leu Leu Asn Asp Leu Val Asp Lys Lys Val Gln Thr Ser Asp Pro 420 425 430 Thr Ser Gly Ile Thr Ile Ser Leu Arg Ala Ala Gln Lys Ser Asn Lys 435 440 445 Leu Lys Asn Asn Val Asp Thr Lys Ala Ser Lys Gly Arg Lys Leu Arg 450 455 460 Tyr His Val Gln Glu Pro Ile Ala Asn Phe Glu Thr Ser Arg Gly Ser 465 470 475 480 <210> SEQ ID NO 39 <211> LENGTH: 558 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 112 <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/NM_000055 <309> DATABASE ENTRY DATE: 2001-02-03 <313> RELEVANT RESIDUES: (1)..(558) <400> SEQUENCE: 39 Met Gly Arg Pro Leu Ala Leu Gln Leu Glu Gln Leu Leu Asn Pro Arg 1 5 10 15 Pro Ser Glu Ala Asp Pro Glu Ala Asp Pro Glu Glu Ala Thr Ala Ala 20 25 30 Arg Val Ile Asp Arg Phe Asp Glu Gly Glu Asp Gly Glu Gly Asp Phe 35 40 45 Leu Val Val Gly Ser Ile Arg Lys Leu Ala Ser Ala Ser Leu Leu Asp 50 55 60 Thr Asp Lys Arg Tyr Cys Gly Lys Thr Thr Ser Arg Lys Ala Trp Asn 65 70 75 80 Glu Asp His Trp Glu Gln Thr Leu Pro Gly Ser Ser Asp Glu Glu Ile 85 90 95 Ser Asp Glu Glu Gly Ser Gly Asp Glu Asp Ser Glu Gly Leu Gly Leu 100 105 110 Glu Glu Tyr Asp Glu Asp Asp Leu Gly Ala Ala Glu Glu Gln Glu Cys 115 120 125 Gly Asp His Arg Glu Ser Lys Lys Thr Arg Ser His Ser Ala Lys Thr 130 135 140 Pro Gly Phe Ser Val Gln Ser Ile Ser Asp Phe Glu Lys Phe Thr Lys 145 150 155 160 Gly Met Asp Asp Leu Gly Ser Ser Glu Glu Glu Glu Asp Glu Glu Ser 165 170 175 Gly Met Glu Glu Gly Asp Asp Ala Glu Asp Ser Gln Gly Glu Ser Glu 180 185 190 Glu Asp Arg Ala Gly Asp Arg Asn Ser Glu Asp Asp Gly Val Val Met 195 200 205 Thr Phe Ser Ser Val Lys Val Ser Glu Glu Val Glu Lys Gly Arg Ala 210 215 220 Val Lys Asn Gln Ile Ala Leu Trp Asp Gln Leu Leu Glu Gly Arg Ile 225 230 235 240 Lys Leu Gln Lys Ala Leu Leu Thr Thr Asn Gln Leu Pro Gln Pro Asp 245 250 255 Val Phe Pro Val Phe Lys Asp Lys Gly Gly Pro Glu Phe Ala Ser Ala 260 265 270 Leu Lys Asn Ser His Lys Ala Leu Lys Ala Leu Leu Arg Ser Leu Val 275 280 285 Gly Leu Gln Glu Glu Leu Leu Phe Gln Tyr Pro Asp Thr Arg Tyr Val 290 295 300 Val Asp Gly Thr Lys Pro Asn Ala Gly Ser Glu Glu Ile Ser Ser Glu 305 310 315 320 Asp Asp Glu Leu Val Glu Glu Lys Lys Gln Gln Arg Arg Arg Val Pro 325 330 335 Ala Lys Arg Lys Leu Glu Met Glu Asp Tyr Pro Ser Phe Met Ala Lys 340 345 350 Ala Leu Pro Thr Leu Gln Ser Thr Gly Thr Thr Leu Gln Lys Trp His 355 360 365 Asp Lys Thr Lys Leu Ala Ser Gly Lys Leu Gly Lys Gly Phe Gly Ala 370 375 380 Phe Glu Arg Ser Ile Leu Thr Gln Ile Asp His Ile Leu Met Cys Lys 385 390 395 400 Glu Arg Leu Leu Arg Arg Thr Gln Thr Lys Arg Ser Val Tyr Arg Val 405 410 415 Leu Gly Lys Pro Glu Pro Ala Ala Gln Pro Val Pro Glu Ser Leu Pro 420 425 430 Gly Glu Pro Glu Ile Leu Pro Gln Ala Pro Ala Asn Ala His Leu Lys 435 440 445 Asp Leu Asp Glu Glu Ile Phe Asp Asp Asp Asp Phe Tyr His Gln Leu 450 455 460 Leu Arg Glu Leu Ile Glu Arg Lys Thr Ser Ser Leu Asp Pro Asn Asp 465 470 475 480 Gln Val Ala His Gly Lys Ala Val Ala Cys Asn Pro Glu Val Thr Glu 485 490 495 Ala Lys Ser Thr Lys Lys Val Asp Arg Lys Ala Ser Lys Gly Arg Lys 500 505 510 Leu Arg Phe His Val Leu Ser Lys Leu Leu Ser Phe Met Ala Pro Ile 515 520 525 Asp His Thr Thr Met Asn Asp Asp Ala Arg Thr Glu Leu Tyr Arg Ser 530 535 540 Leu Phe Gly Gln Leu His Pro Pro Asp Glu Gly His Gly Asp 545 550 555 <210> SEQ ID NO 40 <211> LENGTH: 300 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 113 <400> SEQUENCE: 40 Met Ala Thr Leu His Phe Val Pro Gln His Glu Glu Glu Gln Val Tyr 1 5 10 15 Ser Ile Ser Gly Lys Ala Leu Lys Leu Thr Thr Ser Asp Asp Ile Lys 20 25 30 Pro Tyr Leu Glu Glu Leu Ala Ala Leu Lys Thr Cys Thr Lys Leu Asp 35 40 45 Leu Ser Gly Asn Thr Ile Gly Thr Glu Ala Ser Glu Ala Leu Ala Lys 50 55 60 Cys Ile Ala Glu Asn Thr Gln Val Arg Glu Ser Leu Val Glu Val Asn 65 70 75 80 Phe Ala Asp Leu Tyr Thr Ser Arg Leu Val Asp Glu Val Val Asp Ser 85 90 95 Leu Lys Phe Leu Leu Pro Val Leu Leu Lys Cys Pro His Leu Glu Ile 100 105 110 Val Asn Leu Ser Asp Asn Ala Phe Gly Leu Arg Thr Ile Glu Leu Leu 115 120 125 Glu Asp Tyr Ile Ala His Ala Val Asn Ile Lys His Leu Ile Leu Ser 130 135 140 Asn Asn Gly Met Gly Pro Phe Ala Gly Glu Arg Ile Gly Lys Ala Leu 145 150 155 160 Phe His Leu Ala Gln Asn Lys Lys Ala Ala Ser Lys Pro Phe Leu Glu 165 170 175 Thr Phe Ile Cys Asn Thr Phe Thr Lys His Ala Ser Leu Ile Leu Ala 180 185 190 Lys Ala Leu Pro Thr Trp Lys Asp Ser Leu Phe Glu Leu Asn Leu Asn 195 200 205 Asp Cys Leu Leu Lys Thr Ala Gly Ser Asp Glu Val Phe Lys Val Phe 210 215 220 Thr Glu Val Lys Phe Pro Asn Leu His Val Leu Lys Phe Glu Tyr Asn 225 230 235 240 Glu Met Ala Gln Glu Thr Ile Glu Val Ser Phe Leu Pro Ala Met Glu 245 250 255 Lys Gly Asn Leu Pro Glu Leu Glu Lys Leu Glu Ile Asn Gly Asn Arg 260 265 270 Leu Asp Glu Asp Ser Asp Ala Leu Asp Leu Leu Gln Ser Lys Phe Asp 275 280 285 Asp Leu Glu Val Asp Asp Phe Glu Glu Val Asp Ser 290 295 300 <210> SEQ ID NO 41 <211> LENGTH: 415 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 114 <400> SEQUENCE: 41 Met Ala Ser Val Glu Val Glu Leu Gly Val Thr Pro Glu Thr Thr Tyr 1 5 10 15 Ser Ile Ser Gly Lys Gln Leu Lys Phe Asp Ser Glu Ser Asp Ile Ala 20 25 30 Pro Tyr Ile Lys Glu Leu Thr Glu Lys Glu Asn Val Lys Lys Val Asp 35 40 45 Phe Ser Gly Asn Thr Ile Gly Ile Glu Ala Ser Lys Ala Leu Ser Glu 50 55 60 Ala Leu Leu Lys His Lys Asp Thr Ile Val Glu Ile Asn Phe Ser Asp 65 70 75 80 Leu Tyr Thr Gly Arg Leu Asn Thr Glu Ile Pro Gln Ser Leu Glu Tyr 85 90 95 Leu Leu Pro Ala Leu Ser Lys Leu Pro Asn Leu Lys Leu Ile Asn Leu 100 105 110 Ser Asp Asn Ala Phe Gly Leu Gln Thr Ile Asp Pro Ile Glu Ala Tyr 115 120 125 Leu Ala Lys Ala Val Ser Ile Glu His Leu Ile Leu Ser Asn Asn Gly 130 135 140 Met Gly Pro Phe Ala Gly Ser Arg Ile Gly Gly Ser Leu Phe Lys Leu 145 150 155 160 Ala Lys Ala Lys Lys Ala Glu Gly Lys Glu Ser Leu Lys Thr Phe Ile 165 170 175 Cys Gly Arg Asn Arg Leu Glu Asn Gly Ser Val Asn Tyr Leu Ser Val 180 185 190 Gly Leu Arg Asn His Lys Asp Leu Glu Val Val Arg Leu Tyr Gln Asn 195 200 205 Gly Ile Arg Pro Ala Gly Ile Ser Lys Leu Val Glu Gln Gly Leu Ser 210 215 220 Asn Asn Lys Lys Leu Lys Val Leu Asp Leu Gln Asp Asn Thr Ile Thr 225 230 235 240 Thr Arg Gly Ala Ile His Ile Ala Glu Ser Leu Ser Asn Trp Pro Leu 245 250 255 Leu Val Glu Leu Asn Leu Asn Asp Ser Leu Leu Lys Asn Lys Gly Ser 260 265 270 Leu Lys Leu Val Glu Ala Phe His Ala Gly Asp Glu Lys Pro Gln Leu 275 280 285 Ile Thr Leu Lys Leu Gln Tyr Asn Glu Leu Glu Thr Asp Ser Leu Arg 290 295 300 Val Leu Ala Asp Ala Ile Ala Ser Lys Leu Pro Gln Leu Lys Phe Leu 305 310 315 320 Glu Leu Asn Gly Asn Arg Phe Glu Glu Asp Ser Glu His Ile Asp Lys 325 330 335 Ile Asn Gly Ile Phe Glu Glu Arg Gly Tyr Gly Glu Ile Asp Glu Leu 340 345 350 Asp Glu Leu Glu Glu Leu Asp Ser Glu Glu Glu Glu Asp Asp Glu Asp 355 360 365 Asp Glu Gly Glu Asp Asp Thr Leu Glu Glu Asp Leu Asp Leu Thr Gln 370 375 380 Leu Glu Glu Glu Leu Ala Gly Val Ser Leu Glu Asp Lys Asp Gly Asn 385 390 395 400 Val Asp Glu Ile Ala Glu Glu Leu Ser Lys Thr His Ile Lys Glx 405 410 415 <210> SEQ ID NO 42 <211> LENGTH: 587 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 115 <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/CAA57714 <309> DATABASE ENTRY DATE: 1995-05-11 <313> RELEVANT RESIDUES: (1)..(587) <400> SEQUENCE: 42 Met Ala Ser Glu Asp Ile Ala Lys Leu Ala Glu Thr Leu Ala Lys Thr 1 5 10 15 Gln Val Ala Gly Gly Gln Leu Ser Phe Lys Gly Lys Ser Leu Lys Leu 20 25 30 Asn Thr Ala Glu Asp Ala Lys Asp Val Ile Lys Glu Ile Glu Asp Phe 35 40 45 Asp Ser Leu Glu Ala Leu Arg Leu Glu Gly Asn Thr Val Gly Val Glu 50 55 60 Ala Ala Arg Val Ile Ala Lys Ala Leu Glu Lys Lys Ser Glu Leu Lys 65 70 75 80 Arg Cys His Trp Ser Asp Met Phe Thr Gly Arg Leu Arg Thr Glu Ile 85 90 95 Pro Pro Ala Leu Ile Ser Leu Gly Glu Gly Leu Ile Thr Ala Gly Ala 100 105 110 Gln Leu Val Glu Leu Asp Leu Ser Asp Asn Ala Phe Gly Pro Asp Gly 115 120 125 Val Gln Gly Phe Glu Ala Leu Leu Lys Ser Ser Ala Cys Phe Thr Leu 130 135 140 Gln Glu Leu Lys Leu Asn Asn Cys Gly Met Gly Ile Gly Gly Gly Lys 145 150 155 160 Ile Leu Ala Ala Ala Leu Thr Glu Cys His Arg Lys Ser Ser Ala Gln 165 170 175 Gly Lys Pro Leu Ala Leu Lys Val Phe Val Ala Gly Arg Asn Arg Leu 180 185 190 Glu Asn Asp Gly Ala Thr Ala Leu Ala Glu Ala Phe Arg Val Ile Gly 195 200 205 Thr Leu Glu Glu Val His Met Pro Gln Asn Gly Ile Asn His Pro Gly 210 215 220 Ile Thr Ala Leu Ala Gln Ala Phe Ala Val Asn Pro Leu Leu Arg Val 225 230 235 240 Ile Asn Leu Asn Asp Asn Thr Phe Thr Glu Lys Gly Ala Val Ala Met 245 250 255 Ala Glu Thr Leu Lys Thr Leu Arg Gln Val Glu Val Ile Asn Phe Gly 260 265 270 Asp Cys Leu Val Arg Ser Lys Gly Ala Val Ala Ile Ala Asp Ala Ile 275 280 285 Arg Gly Gly Leu Pro Lys Leu Lys Glu Leu Asn Leu Ser Phe Cys Glu 290 295 300 Ile Lys Arg Asp Ala Ala Leu Ala Val Ala Glu Ala Met Ala Asp Lys 305 310 315 320 Ala Glu Leu Glu Lys Leu Asp Leu Asn Gly Asn Thr Leu Gly Glu Glu 325 330 335 Gly Cys Glu Gln Leu Gln Glu Val Leu Glu Gly Phe Asn Met Ala Lys 340 345 350 Val Leu Ala Ser Leu Ser Asp Asp Glu Asp Glu Glu Glu Glu Glu Glu 355 360 365 Gly Glu Glu Glu Glu Glu Glu Ala Glu Glu Glu Glu Glu Glu Asp Glu 370 375 380 Glu Glu Glu Glu Glu Glu Glu Glu Glu Glu Glu Glu Glu Pro Gln Gln 385 390 395 400 Arg Gly Gln Gly Glu Lys Ser Ala Thr Pro Ser Arg Lys Ile Leu Asp 405 410 415 Pro Asn Thr Gly Glu Pro Ala Pro Val Leu Ser Ser Pro Pro Pro Ala 420 425 430 Asp Val Ser Thr Phe Leu Ala Phe Pro Ser Pro Glu Lys Leu Leu Arg 435 440 445 Leu Gly Pro Lys Ser Ser Val Leu Ile Ala Gln Gln Thr Asp Thr Ser 450 455 460 Asp Pro Glu Lys Val Val Ser Ala Phe Leu Lys Val Ser Ser Val Phe 465 470 475 480 Lys Asp Glu Ala Thr Val Arg Met Ala Val Gln Asp Ala Val Asp Ala 485 490 495 Leu Met Gln Lys Ala Phe Asn Ser Ser Ser Phe Asn Ser Asn Thr Phe 500 505 510 Leu Thr Arg Leu Leu Val His Met Gly Leu Leu Lys Ser Glu Asp Lys 515 520 525 Val Lys Ala Ile Ala Asn Leu Tyr Gly Pro Leu Met Ala Leu Asn His 530 535 540 Met Val Gln Gln Asp Tyr Phe Pro Lys Ala Leu Ala Pro Leu Leu Leu 545 550 555 560 Ala Phe Val Thr Lys Pro Asn Ser Ala Leu Glu Ser Cys Ser Phe Ala 565 570 575 Arg His Ser Leu Leu Gln Thr Leu Tyr Lys Val 580 585 <210> SEQ ID NO 43 <211> LENGTH: 381 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 116 <400> SEQUENCE: 43 Met Ser Ser Gln Ala Phe Thr Ser Val His Pro Asn Ala Ala Thr Ser 1 5 10 15 Asp Val Asn Val Thr Ile Asp Thr Phe Val Ala Lys Leu Lys Arg Arg 20 25 30 Gln Val Gln Gly Ser Tyr Ala Ile Ala Leu Glu Thr Leu Gln Leu Leu 35 40 45 Met Arg Phe Ile Ser Ala Ala Arg Trp Asn His Val Asn Asp Leu Ile 50 55 60 Glu Gln Ile Arg Asp Leu Gly Asn Ser Leu Glu Lys Ala His Pro Thr 65 70 75 80 Ala Phe Ser Cys Gly Asn Val Ile Arg Arg Ile Leu Ala Val Leu Arg 85 90 95 Asp Glu Val Glu Glu Asp Thr Met Ser Thr Thr Val Thr Ser Thr Ser 100 105 110 Val Ala Glu Pro Leu Ile Ser Ser Met Phe Asn Leu Leu Gln Lys Pro 115 120 125 Glu Gln Pro His Gln Asn Arg Lys Asn Ser Ser Gly Ser Ser Ser Met 130 135 140 Lys Thr Lys Thr Asp Tyr Arg Gln Val Ala Ile Gln Gly Ile Lys Asp 145 150 155 160 Leu Ile Asp Glu Ile Lys Asn Ile Asp Glu Gly Ile Gln Gln Ile Ala 165 170 175 Ile Asp Leu Ile His Asp His Glu Ile Leu Leu Thr Pro Thr Pro Asp 180 185 190 Ser Lys Thr Val Leu Lys Phe Leu Ile Thr Ala Arg Glu Arg Ser Asn 195 200 205 Arg Thr Phe Thr Val Leu Val Thr Glu Gly Phe Pro Asn Asn Thr Lys 210 215 220 Asn Ala His Glu Phe Ala Lys Lys Leu Ala Gln His Asn Ile Glu Thr 225 230 235 240 Leu Val Val Pro Asp Ser Ala Val Phe Ala Leu Met Ser Arg Val Gly 245 250 255 Lys Val Ile Ile Gly Thr Lys Ala Val Phe Val Asn Gly Gly Thr Ile 260 265 270 Ser Ser Asn Ser Gly Val Ser Ser Val Cys Glu Cys Ala Arg Glu Phe 275 280 285 Arg Thr Pro Val Phe Ala Val Ala Gly Leu Tyr Lys Leu Ser Pro Leu 290 295 300 Tyr Pro Phe Asp Val Glu Lys Phe Val Glu Phe Gly Gly Ser Gln Arg 305 310 315 320 Ile Leu Pro Arg Met Asp Pro Arg Lys Arg Leu Asp Thr Val Asn Gln 325 330 335 Ile Thr Asp Tyr Val Pro Pro Glu Asn Ile Asp Ile Tyr Ile Thr Asn 340 345 350 Val Gly Gly Phe Asn Pro Ser Phe Ile Tyr Arg Ile Ala Trp Asp Asn 355 360 365 Tyr Lys Gln Ile Asp Val His Leu Asp Lys Asn Lys Ala 370 375 380 <210> SEQ ID NO 44 <211> LENGTH: 365 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 117 <400> SEQUENCE: 44 Met Ser Lys Leu Leu Thr Pro Glu Ile Leu Ala Leu Ile Asp Pro Val 1 5 10 15 Val Ser Ser Leu Lys Arg His Gln Leu Val Asp Asp Lys Glu Ile Ala 20 25 30 Leu Thr Ile Ala Gln Leu Leu Met Lys Val Ile Ser Ala Ala Arg Trp 35 40 45 Ser Asn Thr Tyr Asp Leu Ile Glu Leu Ile Arg Gln Val Gly Val Ile 50 55 60 Phe Thr Glu Ala Tyr Pro Arg Lys Val Ile Pro Gly Asn Ile Val Arg 65 70 75 80 Arg Val Leu Ala Leu Ile Arg Asp Glu Thr Glu Thr Glu Thr Glu Thr 85 90 95 Glu Thr Glu Gln Thr Asp Asn Ile Pro Met Met Ser Ser Met Phe Ser 100 105 110 Leu Leu Ala Thr His Asn Lys Asn Glu Thr Ile Lys Glu Gln Thr Gln 115 120 125 Leu Gln Leu Lys Lys Gln Thr Ser Asp Met Arg Ala Ile Ile Ile Gln 130 135 140 Gly Ile Arg Asp Leu Val Asp Glu Ile Ser Asn Val Asn Asp Gly Ile 145 150 155 160 Glu Thr Met Ala Val Asp Leu Ile His Asp Asp Glu Ile Leu Leu Thr 165 170 175 Pro Thr Pro Asn Ser Glu Thr Val Gln His Phe Leu Ile Lys Ala Arg 180 185 190 Leu Lys Arg Lys Phe Thr Val Val Val Thr Glu Asn Tyr Pro Asn Asp 195 200 205 Ile Lys Ala Ala His Lys Phe Val Lys Thr Leu Ala Glu His Asn Ile 210 215 220 Glu Thr Ile Leu Ile Pro Asp Thr Thr Ile Tyr Ala Val Met Ser Arg 225 230 235 240 Val Gly Lys Val Ile Ile Gly Thr Asn Ala Val Phe Ala Asn Gly Gly 245 250 255 Cys Leu Ser Asn Ser Gly Val Ala Asn Val Val Glu Cys Ala Lys Glu 260 265 270 His Arg Thr Pro Val Phe Ala Val Ala Gly Leu Phe Lys Leu Ser Pro 275 280 285 Leu Tyr Pro Phe Thr Arg Asn Asp Leu Ile Glu Val Gly Asn Ser Gly 290 295 300 Lys Val Leu Asn Tyr Asp Asp Phe Glu Leu Val Gln Asn Val Asp Val 305 310 315 320 Val Thr Asn Pro Leu Glu Asp Tyr Ile Pro Pro Gln His Ile Asp Ile 325 330 335 Phe Met Thr Asn Ile Gly Gly Phe Ser Pro Ser Phe Ile Tyr Arg Ile 340 345 350 Val Leu Asp Asn Tyr Lys Ala Glu Asp Asn Lys Leu Glu 355 360 365 <210> SEQ ID NO 45 <211> LENGTH: 349 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 118 <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/AAC42002 <309> DATABASE ENTRY DATE: 1995-07-14 <313> RELEVANT RESIDUES: (1)..(349) <400> SEQUENCE: 45 Met Pro Gly Ser Ala Ala Lys Gly Ser Glu Leu Ser Glu Arg Ile Glu 1 5 10 15 Ser Phe Val Glu Thr Leu Lys Arg Gly Gly Gly Pro Arg Ser Ser Glu 20 25 30 Glu Met Ala Arg Glu Thr Leu Gly Leu Leu Arg Gln Ile Ile Thr Asp 35 40 45 His Arg Trp Ser Asn Ala Gly Glu Leu Met Glu Leu Ile Arg Arg Glu 50 55 60 Gly Arg Arg Met Thr Ala Ala Gln Pro Ser Glu Thr Thr Val Gly Asn 65 70 75 80 Met Val Arg Arg Val Leu Lys Ile Ile Arg Glu Glu Tyr Gly Arg Leu 85 90 95 His Gly Arg Ser Asp Glu Asp Gln Gln Glu Ser Leu His Lys Leu Leu 100 105 110 Thr Ser Gly Gly Leu Asn Glu Asp Phe Ser Phe His Tyr Ala Gln Leu 115 120 125 Gln Ser Asn Ile Ile Glu Ala Ile Asn Glu Leu Leu Val Glu Leu Glu 130 135 140 Gly Thr Met Glu Asn Ile Ala Ala Gln Ala Leu Glu His Ile His Ser 145 150 155 160 Asn Glu Val Ile Met Thr Ile Gly Phe Ser Arg Thr Val Glu Ala Phe 165 170 175 Leu Lys Glu Ala Ala Arg Lys Arg Lys Phe His Val Ile Val Ala Glu 180 185 190 Cys Ala Pro Phe Cys Gln Gly His Glu Met Ala Val Asn Leu Ser Lys 195 200 205 Ala Gly Ile Glu Thr Thr Val Met Thr Ala Ala Ile Phe Ala Val Met 210 215 220 Ser Arg Val Asn Lys Val Ile Ile Gly Thr Lys Thr Ile Leu Ala Asn 225 230 235 240 Gly Ala Leu Arg Ala Val Thr Gly Thr His Thr Leu Ala Leu Ala Ala 245 250 255 Lys His His Ser Thr Pro Leu Ile Val Cys Ala Pro Met Phe Lys Leu 260 265 270 Ser Pro Gln Phe Pro Asn Glu Glu Asp Ser Phe His Lys Phe Val Ala 275 280 285 Pro Glu Glu Val Leu Pro Phe Thr Glu Gly Asp Ile Leu Glu Lys Val 290 295 300 Ser Val His Cys Pro Val Phe Asp Tyr Val Pro Pro Glu Leu Ile Thr 305 310 315 320 Leu Phe Ile Ser Asn Ile Gly Gly Asn Ala Pro Ser Tyr Ile Tyr Arg 325 330 335 Leu Met Ser Glu Leu Tyr His Pro Asp Asp His Val Leu 340 345 <210> SEQ ID NO 46 <211> LENGTH: 246 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 119 <400> SEQUENCE: 46 Met Ser Arg Leu Glu Ile Tyr Ser Pro Glu Gly Leu Arg Leu Asp Gly 1 5 10 15 Arg Arg Trp Asn Glu Leu Arg Arg Phe Glu Ser Ser Ile Asn Thr His 20 25 30 Pro His Ala Ala Asp Gly Ser Ser Tyr Met Glu Gln Gly Asn Asn Lys 35 40 45 Ile Ile Thr Leu Val Lys Gly Pro Lys Glu Pro Arg Leu Lys Ser Gln 50 55 60 Met Asp Thr Ser Lys Ala Leu Leu Asn Val Ser Val Asn Ile Thr Lys 65 70 75 80 Phe Ser Lys Phe Glu Arg Ser Lys Ser Ser His Lys Asn Glu Arg Arg 85 90 95 Val Leu Glu Ile Gln Thr Ser Leu Val Arg Met Phe Glu Lys Asn Val 100 105 110 Met Leu Asn Ile Tyr Pro Arg Thr Val Ile Asp Ile Glu Ile His Val 115 120 125 Leu Glu Gln Asp Gly Gly Ile Met Gly Ser Leu Ile Asn Gly Ile Thr 130 135 140 Leu Ala Leu Ile Asp Ala Gly Ile Ser Met Phe Asp Tyr Ile Ser Gly 145 150 155 160 Ile Ser Val Gly Leu Tyr Asp Thr Thr Pro Leu Leu Asp Thr Asn Ser 165 170 175 Leu Glu Glu Asn Ala Met Ser Thr Val Thr Leu Gly Val Val Gly Lys 180 185 190 Ser Glu Lys Leu Ser Leu Leu Leu Val Glu Asp Lys Ile Pro Leu Asp 195 200 205 Arg Leu Glu Asn Val Leu Ala Ile Gly Ile Ala Gly Ala His Arg Val 210 215 220 Arg Asp Leu Met Asp Glu Glu Leu Arg Lys His Ala Gln Lys Arg Val 225 230 235 240 Ser Asn Ala Ser Ala Arg 245 <210> SEQ ID NO 47 <211> LENGTH: 180 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 120 <400> SEQUENCE: 47 Met Glu Leu Tyr Ser Pro Glu Gly Leu Arg Ile Asp Gly Arg Arg Trp 1 5 10 15 Asn Glu Leu Arg Arg Phe Glu Cys Arg Ile Asn Thr His Pro Asn Ser 20 25 30 Ser Asp Gly Ser Ser Tyr Val Glu Gln Gly Asn Thr Lys Val Met Cys 35 40 45 Thr Val Gln Gly Pro Ile Glu Pro Ala Leu Arg Ser Gln Gln His Ser 50 55 60 Glu Arg Ala Asn Ile Glu Val Asn Leu Asn Ile Ala Ser Phe Ser Thr 65 70 75 80 Phe Glu Arg Lys Lys Arg Ser Arg Asn Glu Arg Arg Leu Val Glu Leu 85 90 95 Lys Thr Thr Leu Glu Lys Thr Phe Glu Glu Ser Val Met Ile Asn Leu 100 105 110 Tyr Pro Arg Thr Asn Ile Val Ile Asn Val Gln Val Leu Cys Gln Asp 115 120 125 Gly Gly Met Leu Ala Ala Val Ile Asn Ser Ile Thr Leu Ala Leu Ile 130 135 140 Asp Ala Gly Ile Ser Met Tyr Asp Tyr Val Ser Gly Val Ser Cys Gly 145 150 155 160 Leu Tyr Asp Gln Thr Pro Leu Leu Asp Val Asn Asn Leu Glu Glu His 165 170 175 Asp Met Ser Cys 180 <210> SEQ ID NO 48 <211> LENGTH: 245 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 121 <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/BAA91279 <309> DATABASE ENTRY DATE: 2000-02-22 <313> RELEVANT RESIDUES: (1)..(245) <400> SEQUENCE: 48 Met Ala Gly Leu Glu Leu Leu Ser Asp Gln Gly Tyr Arg Val Asp Gly 1 5 10 15 Arg Arg Ala Gly Glu Leu Arg Lys Ile Gln Ala Arg Met Gly Val Phe 20 25 30 Ala Gln Ala Asp Gly Ser Ala Tyr Ile Glu Gln Gly Asn Thr Lys Ala 35 40 45 Leu Ala Val Val Tyr Gly Pro His Glu Ile Arg Ser Arg Ala Arg Ala 50 55 60 Leu Pro Asp Arg Ala Leu Val Asn Cys Gln Tyr Ser Ser Ala Thr Phe 65 70 75 80 Ser Thr Gly Glu Arg Lys Arg Arg Pro His Gly Asp Arg Lys Ser Cys 85 90 95 Glu Met Gly Leu Gln Leu Arg Gln Thr Phe Glu Ala Ala Ile Leu Thr 100 105 110 Gln Leu His Pro Arg Ser Gln Ile Asp Ile Tyr Val Gln Val Leu Gln 115 120 125 Ala Asp Gly Gly Thr Tyr Ala Ala Cys Val Asn Ala Ala Thr Leu Ala 130 135 140 Val Leu Asp Ala Gly Ile Pro Met Arg Asp Phe Val Cys Ala Cys Ser 145 150 155 160 Ala Gly Phe Val Asp Gly Thr Ala Leu Ala Asp Leu Ser His Val Glu 165 170 175 Glu Ala Ala Gly Gly Pro Gln Leu Ala Leu Ala Leu Leu Pro Ala Ser 180 185 190 Gly Gln Ile Ala Leu Leu Glu Met Asp Ala Arg Leu His Glu Asp His 195 200 205 Leu Glu Arg Val Leu Glu Ala Ala Ala Gln Ala Ala Arg Asp Val His 210 215 220 Thr Leu Leu Asp Arg Val Val Arg Gln His Val Arg Glu Ala Ser Ile 225 230 235 240 Leu Leu Gly Asp Gly 245 <210> SEQ ID NO 49 <211> LENGTH: 720 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 122 <400> SEQUENCE: 49 Met Ser Arg Phe Phe Ser Ser Asn Tyr Glu Tyr Asp Val Ala Ser Ser 1 5 10 15 Ser Ser Glu Glu Asp Leu Leu Ser Ser Ser Glu Glu Asp Leu Leu Ser 20 25 30 Ser Ser Ser Ser Glu Ser Glu Leu Asp Gln Glu Ser Asp Asp Ser Phe 35 40 45 Phe Asn Glu Ser Glu Ser Glu Ser Glu Ala Asp Val Asp Ser Asp Asp 50 55 60 Ser Asp Ala Lys Pro Tyr Gly Pro Asp Trp Phe Lys Lys Ser Glu Phe 65 70 75 80 Arg Lys Gln Gly Gly Gly Ser Asn Lys Phe Leu Lys Ser Ser Asn Tyr 85 90 95 Asp Ser Ser Asp Glu Glu Ser Asp Glu Glu Asp Gly Lys Lys Val Val 100 105 110 Lys Ser Ala Lys Glu Lys Leu Leu Asp Glu Met Gln Asp Val Tyr Asn 115 120 125 Lys Ile Ser Gln Ala Glu Asn Ser Asp Asp Trp Leu Thr Ile Ser Asn 130 135 140 Glu Phe Asp Leu Ile Ser Arg Leu Leu Val Arg Ala Gln Gln Gln Asn 145 150 155 160 Trp Gly Thr Pro Asn Ile Phe Ile Lys Val Val Ala Gln Val Glu Asp 165 170 175 Ala Val Asn Asn Thr Gln Gln Ala Asp Leu Lys Asn Lys Ala Val Ala 180 185 190 Arg Ala Tyr Asn Thr Thr Lys Gln Arg Val Lys Lys Val Ser Arg Glu 195 200 205 Asn Glu Asp Ser Met Ala Lys Phe Arg Asn Asp Pro Glu Ser Phe Asp 210 215 220 Lys Glu Pro Thr Ala Asp Leu Asp Ile Ser Ala Asn Gly Phe Thr Ile 225 230 235 240 Ser Ser Ser Gln Gly Asn Asp Gln Ala Val Gln Glu Asp Phe Phe Thr 245 250 255 Arg Leu Gln Thr Ile Ile Asp Ser Arg Gly Lys Lys Thr Val Asn Gln 260 265 270 Gln Ser Leu Ile Ser Thr Leu Glu Glu Leu Leu Thr Val Ala Glu Lys 275 280 285 Pro Tyr Glu Phe Ile Met Ala Tyr Leu Thr Leu Ile Pro Ser Arg Phe 290 295 300 Asp Ala Ser Ala Asn Leu Ser Tyr Gln Pro Ile Asp Gln Trp Lys Ser 305 310 315 320 Ser Phe Asn Asp Ile Ser Lys Leu Leu Ser Ile Leu Asp Gln Thr Ile 325 330 335 Asp Thr Tyr Gln Val Asn Glu Phe Ala Asp Pro Ile Asp Phe Ile Glu 340 345 350 Asp Glu Pro Lys Glu Asp Ser Asp Gly Val Lys Arg Ile Leu Gly Ser 355 360 365 Ile Phe Ser Phe Val Glu Arg Leu Asp Asp Glu Phe Met Lys Ser Leu 370 375 380 Leu Asn Ile Asp Pro His Ser Ser Asp Tyr Leu Ile Arg Leu Arg Asp 385 390 395 400 Glu Gln Ser Ile Tyr Asn Leu Ile Leu Arg Thr Gln Leu Tyr Phe Glu 405 410 415 Ala Thr Leu Lys Asp Glu His Asp Leu Glu Arg Ala Leu Thr Arg Pro 420 425 430 Phe Val Lys Arg Leu Asp His Ile Tyr Tyr Lys Ser Glu Asn Leu Ile 435 440 445 Lys Ile Met Glu Thr Ala Ala Trp Asn Ile Ile Pro Ala Gln Phe Lys 450 455 460 Ser Lys Phe Thr Ser Lys Asp Gln Leu Asp Ser Ala Asp Tyr Val Asp 465 470 475 480 Asn Leu Ile Asp Gly Leu Ser Thr Ile Leu Ser Lys Gln Asn Asn Ile 485 490 495 Ala Val Gln Lys Arg Ala Ile Leu Tyr Asn Ile Tyr Tyr Thr Ala Leu 500 505 510 Asn Lys Asp Phe Gln Thr Ala Lys Asp Met Leu Leu Thr Ser Gln Val 515 520 525 Gln Thr Asn Ile Asn Gln Phe Asp Ser Ser Leu Gln Ile Leu Phe Asn 530 535 540 Arg Val Val Val Gln Leu Gly Leu Ser Ala Phe Lys Leu Cys Leu Ile 545 550 555 560 Glu Glu Cys His Gln Ile Leu Asn Asp Leu Leu Ser Ser Ser His Leu 565 570 575 Arg Glu Ile Leu Gly Gln Gln Ser Leu His Arg Ile Ser Leu Asn Ser 580 585 590 Ser Asn Asn Ala Ser Ala Asp Glu Arg Ala Arg Gln Cys Leu Pro Tyr 595 600 605 His Gln His Ile Asn Leu Asp Leu Ile Asp Val Val Phe Leu Thr Cys 610 615 620 Ser Leu Leu Ile Glu Ile Pro Arg Met Thr Ala Phe Tyr Ser Gly Ile 625 630 635 640 Lys Val Lys Arg Ile Pro Tyr Ser Pro Lys Ser Ile Arg Arg Ser Leu 645 650 655 Glu His Tyr Asp Ser Leu Lys Thr Tyr Phe Phe Ser Phe Lys Arg Phe 660 665 670 Tyr Ser Ser Phe Ser Val Ala Lys Leu Ala Glu Leu Phe Asp Leu Pro 675 680 685 Glu Asn Lys Val Val Glu Val Leu Gln Ser Val Ile Ala Glu Leu Glu 690 695 700 Ile Pro Ala Lys Leu Asn Asp Glu Lys Thr Ile Phe Val Val Glu Lys 705 710 715 720 <210> SEQ ID NO 50 <211> LENGTH: 874 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 123 <400> SEQUENCE: 50 Met Ser Arg Phe Phe Val Ser Gly Tyr Thr Ser Asp Ser Ser Ser Glu 1 5 10 15 Glu Glu Asp Leu Leu Ser Thr Ser Glu Glu Glu Leu Leu Ser Ser Ser 20 25 30 Asp Glu Gly Glu Asp Asn Glu Ser Asp Ser Ser Phe Phe Gly Glu Asp 35 40 45 Asp Asp Glu Ser Glu Glu Ser Ser Ser Asp Asp Glu Asp Gly Arg Pro 50 55 60 Ser Gly Pro Ala Tyr Phe Leu Lys Lys Ser Phe Leu Lys Gly Ala Gly 65 70 75 80 Gly Asp Asp Ser Asp Ser Asp Ser Asp Asp Glu Gly Arg Lys Val Val 85 90 95 Lys Ser Ala Lys Asp Lys Leu Leu Asp Asp Met Lys Ser Ser Ile Glu 100 105 110 Ile Ile Asn Ser Asn Lys Tyr Asn Asn Asn Trp Ser Ile Val Leu Gly 115 120 125 Glu Phe Asp Lys Phe Gly Arg Phe Leu Ile Arg Cys Asn Gln Thr Asn 130 135 140 Leu Gly Thr Pro Lys Phe Tyr Ile Lys Leu Leu Thr Ser Leu Asp Asn 145 150 155 160 Ser Ile Thr Glu Thr Ser Asn Asn Glu Arg Asp Asp Lys Thr Leu Lys 165 170 175 Ala Asp Glu Ala Arg Ala Phe Asn Thr Leu Arg Gln Arg Ile Lys Lys 180 185 190 Gln Ile Arg Glu Phe Gln Val Tyr Tyr Asp Leu Tyr Lys Glu Asn Pro 195 200 205 Glu Glu Phe Asp Glu Asn Glu Asp Glu Pro Leu Glu Ser Val Gln Ala 210 215 220 Gly Leu Asn Asp Asn Val Lys Asn Glu Ala Asp Asn Ser Asn Val Gly 225 230 235 240 Ala Leu Ala Ser Asn Arg Val Leu Ser Pro Ile Phe His Thr Leu Lys 245 250 255 Thr Ile Ser Glu Ser Arg Gly Lys Lys Asn Ile Asp Lys Leu Glu Gln 260 265 270 Ile Ala Thr Leu Glu Lys Leu Leu Glu Ala Asn Val Ser Lys Ser Ser 275 280 285 Pro Phe Glu Leu Ile Ser Ile Tyr Gln Met Leu Leu Ser Val Arg Phe 290 295 300 Asp Ala Ser Ser Asn Gln Ala Phe Met Pro Leu Glu Gln Trp Gln Lys 305 310 315 320 Asn Glu His Asp Leu Gly Lys Leu Leu Asp Leu Leu Glu Ala Asn Val 325 330 335 Asp Thr Tyr Gln Val Ser Glu Leu Gly Ser Thr Thr Asp Asp Ile Asp 340 345 350 Ile Glu Pro Val Ala Asn Ala Gln Gly Val Lys Val Ile Phe Gly Ser 355 360 365 Ile Thr Ser Ser Ile Asp Arg Leu Asp Asp Glu Leu Thr Lys Ser Leu 370 375 380 Gln His Thr Asp Pro His Ser Ile Glu Tyr Val Glu Arg Leu Lys Asp 385 390 395 400 Glu Ser Thr Ile Tyr Asn Leu Ile Val Arg Gly Gln Ala Tyr Val Glu 405 410 415 Ser Ile Thr Pro Glu Asp Val Lys Tyr Asn Ser Glu Gln Leu Ala Arg 420 425 430 Ile Val Leu Arg Arg Leu Glu His Ile Tyr Tyr Lys Pro Lys Gln Leu 435 440 445 Ile Lys Ala Asn Glu Glu Glu Ala Trp Arg Asn Ile Glu Tyr Asn Ser 450 455 460 Ser Ile Val Ser Lys Gly Ser Ser Val Asp Glu Val Ile Asp Gln Leu 465 470 475 480 Thr Glu Phe Leu Gln Lys Gln Gln Lys Asn Lys Thr Tyr Gly Lys His 485 490 495 Ala Ile Leu Phe Ser Ile Tyr Tyr Tyr Ala Val Asn Ser Gln Tyr Glu 500 505 510 Lys Ala Lys Glu Leu Phe Leu Arg Ser Gln Phe Tyr Ser Asn Ile Asn 515 520 525 Ser Ala Glu Ser Ser Leu Gln Val Gln Tyr Asn Arg Ala Leu Val Gln 530 535 540 Leu Gly Leu Ser Ala Phe Arg Ala Gly Ser Ile Glu Glu Ser His Lys 545 550 555 560 Ile Leu Asn Glu Ile Val Asn Ser Gln Arg Ser Lys Glu Leu Leu Gly 565 570 575 Gln Gly Phe Asn Ser Lys Phe Pro Asn Gln Ala Thr Val Leu Glu Arg 580 585 590 Gln Lys Leu Leu Pro Phe His Gln His Ile Asn Leu Glu Leu Leu Glu 595 600 605 Cys Val Phe Met Thr Cys Ser Leu Leu Ile Glu Ile Pro Thr Leu Ala 610 615 620 Ala Ile Ala Asn Asn His Lys Asp Ser Lys Arg Lys Asn Ala Ser Leu 625 630 635 640 Lys Ser Phe Lys Ser Lys Leu Asp Phe His Asp Arg Gln Phe Phe Thr 645 650 655 Gly Pro Pro Glu Ser Ile Lys Asp His Ile Val His Ala Ser Ile Ala 660 665 670 Leu Gln Lys Gly Asp Trp Leu Lys Ser Tyr Asn Leu Leu Ser Ser Ile 675 680 685 Lys Ile Trp Lys Leu Phe Pro Asp Asn Asp Lys Leu Leu Ala Met Met 690 695 700 Lys Asn Gln Leu Gln Ile Glu Gly Leu Arg Thr Tyr Ile Phe Thr Tyr 705 710 715 720 Lys Ser Val Phe Lys Lys Leu Ser Ile Glu Lys Leu Gln Gln Ile Phe 725 730 735 Gln Leu Ser Lys Asp Glu Val Val Ser Ile Leu Glu Lys Met Ile Thr 740 745 750 Thr Gly Asn Val Ser Gly Gly Glu Ile Ile Asp Asn Lys Phe Ile Ser 755 760 765 Phe Thr Ser Thr Thr Glu Pro Gln Arg Ser Lys Leu Gln Glu Leu Ala 770 775 780 Ile Val Leu Asn Glu Lys Ile Gln Leu Leu Thr Glu Lys Asn Glu Lys 785 790 795 800 Thr Gln Ser Asn Gly Tyr Gly Lys Lys Gln Gln Asn Lys Asp Gln Gln 805 810 815 Asn Gln Gln Gln Gln Asn Gln Asn Gln Asn Gln Gln Gln Gln Gln Asn 820 825 830 Gln Gln Gln Gln Gln Gln Gln Gln Ser Ser Gln Gln Gln Ser Asn Asn 835 840 845 Ile Leu Ser Glu Glu Ser Ala Asn Lys Phe Arg Tyr Ala Asn Val Asn 850 855 860 Ser Asn Asn Asp Glu Phe Gln Ala Thr Ala 865 870 <210> SEQ ID NO 51 <211> LENGTH: 853 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 124 <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/AAD03462 <309> DATABASE ENTRY DATE: 1999-01-08 <313> RELEVANT RESIDUES: (1)..(853) <400> SEQUENCE: 51 Met Ser Arg Phe Phe Thr Thr Gly Ser Asp Ser Glu Ser Glu Ser Ser 1 5 10 15 Leu Ser Gly Glu Glu Leu Val Thr Lys Pro Val Gly Gly Asn Tyr Gly 20 25 30 Lys Gln Pro Leu Leu Leu Ser Glu Asp Glu Glu Asp Thr Lys Arg Val 35 40 45 Val Arg Ser Ala Lys Asp Lys Arg Phe Glu Glu Leu Thr Asn Leu Ile 50 55 60 Arg Thr Ile Arg Asn Ala Met Lys Ile Arg Asp Val Thr Lys Cys Leu 65 70 75 80 Glu Glu Phe Glu Leu Leu Gly Lys Ala Tyr Gly Lys Ala Lys Ser Ile 85 90 95 Val Asp Lys Glu Gly Val Pro Arg Phe Tyr Ile Arg Ile Leu Ala Asp 100 105 110 Leu Glu Asp Tyr Leu Asn Glu Leu Trp Glu Asp Lys Glu Gly Lys Lys 115 120 125 Lys Met Asn Lys Asn Asn Ala Lys Ala Leu Ser Thr Leu Arg Gln Lys 130 135 140 Ile Arg Lys Tyr Asn Arg Asp Phe Glu Ser His Ile Thr Ser Tyr Lys 145 150 155 160 Gln Asn Pro Glu Gln Ser Ala Asp Glu Asp Ala Glu Lys Asn Glu Glu 165 170 175 Asp Ser Glu Gly Ser Ser Asp Glu Asp Glu Asp Glu Asp Gly Val Ser 180 185 190 Ala Ala Thr Phe Leu Lys Lys Lys Ser Glu Ala Pro Ser Gly Glu Ser 195 200 205 Arg Lys Phe Leu Lys Lys Met Asp Asp Glu Asp Glu Asp Ser Glu Asp 210 215 220 Ser Glu Asp Asp Glu Asp Trp Asp Thr Gly Ser Thr Ser Ser Asp Ser 225 230 235 240 Asp Ser Glu Glu Glu Glu Gly Lys Gln Thr Ala Leu Ala Ser Arg Phe 245 250 255 Leu Lys Lys Ala Pro Thr Thr Asp Glu Asp Lys Lys Ala Ala Glu Lys 260 265 270 Lys Arg Glu Asp Lys Ala Lys Lys Lys His Asp Arg Lys Ser Lys Arg 275 280 285 Leu Asp Glu Glu Glu Glu Asp Asn Glu Gly Gly Glu Ala Ala Glu Asn 290 295 300 Asn Leu Gly Glu Gly Val Ile Val Lys Ile Lys Phe Asn Ile Ile Ala 305 310 315 320 Ser Leu Tyr Asp Tyr Asn Pro Asn Leu Ala Thr Tyr Met Lys Pro Glu 325 330 335 Met Trp Gly Lys Cys Leu Asp Cys Ile Asn Glu Leu Met Asp Ile Leu 340 345 350 Phe Ala Asn Pro Asn Ile Phe Val Gly Glu Asn Ile Leu Glu Glu Ser 355 360 365 Glu Asn Leu His Asn Ala Asp Gln Pro Leu Arg Val Arg Gly Cys Ile 370 375 380 Leu Thr Leu Val Glu Arg Met Asp Glu Glu Phe Thr Lys Ile Met Gln 385 390 395 400 Asn Thr Asp Pro His Ser Gln Glu Tyr Val Glu His Leu Lys Asp Glu 405 410 415 Ala Gln Val Cys Ala Ile Ile Glu Arg Val Gln Arg Tyr Leu Glu Glu 420 425 430 Lys Gly Thr Thr Glu Glu Val Cys Arg Ile Tyr Leu Leu Arg Ile Leu 435 440 445 His Thr Tyr Tyr Lys Phe Asp Tyr Lys Ala His Gln Arg Gln Leu Thr 450 455 460 Pro Pro Glu Gly Ser Ser Lys Ser Glu Gln Asp Gln Ala Glu Asn Glu 465 470 475 480 Gly Glu Asp Ser Ala Val Leu Met Glu Arg Leu Cys Lys Tyr Ile Tyr 485 490 495 Ala Lys Asp Arg Thr Asp Arg Ile Arg Thr Cys Ala Ile Leu Cys His 500 505 510 Ile Tyr His His Ala Leu His Ser Arg Trp Tyr Gln Ala Arg Asp Leu 515 520 525 Met Leu Met Ser His Leu Gln Asp Asn Ile Gln His Ala Asp Pro Pro 530 535 540 Val Gln Ile Leu Tyr Asn Arg Thr Met Val Gln Leu Gly Ile Cys Ala 545 550 555 560 Phe Arg Gln Gly Leu Thr Lys Asp Ala His Asn Ala Leu Leu Asp Ile 565 570 575 Gln Ser Ser Gly Arg Ala Lys Glu Leu Leu Gly Gln Gly Leu Leu Leu 580 585 590 Arg Ser Leu Gln Glu Arg Asn Gln Glu Gln Glu Lys Val Glu Arg Arg 595 600 605 Arg Gln Val Pro Phe His Leu His Ile Asn Leu Glu Leu Leu Glu Cys 610 615 620 Val Tyr Leu Val Ser Ala Met Leu Leu Glu Ile Pro Tyr Met Ala Ala 625 630 635 640 His Glu Ser Asp Ala Arg Arg Arg Met Ile Ser Lys Gln Phe His His 645 650 655 Gln Leu Arg Val Gly Glu Arg Gln Pro Leu Leu Gly Pro Pro Glu Ser 660 665 670 Met Arg Glu His Val Val Ala Ala Ser Lys Ala Met Lys Met Gly Asp 675 680 685 Trp Lys Thr Cys His Ser Phe Ile Ile Asn Glu Lys Met Asn Gly Lys 690 695 700 Val Trp Asp Leu Phe Pro Glu Ala Asp Lys Val Arg Thr Met Leu Val 705 710 715 720 Arg Lys Ile Gln Glu Glu Ser Leu Arg Thr Tyr Leu Phe Thr Tyr Ser 725 730 735 Ser Val Tyr Asp Ser Ile Ser Met Glu Thr Leu Ser Asp Met Phe Glu 740 745 750 Leu Asp Leu Pro Thr Val His Ser Ile Ile Ser Lys Met Ile Ile Asn 755 760 765 Glu Glu Leu Met Ala Ser Leu Asp Gln Pro Thr Gln Thr Val Val Met 770 775 780 His Arg Thr Glu Pro Thr Ala Gln Gln Asn Leu Ala Leu Gln Leu Ala 785 790 795 800 Glu Lys Leu Gly Ser Leu Val Glu Asn Asn Glu Arg Val Phe Asp His 805 810 815 Lys Gln Gly Thr Tyr Gly Gly Tyr Phe Arg Asp Gln Lys Asp Gly Tyr 820 825 830 Arg Lys Asn Glu Gly Tyr Met Arg Arg Gly Gly Tyr Arg Gln Gln Gln 835 840 845 Ser Gln Thr Ala Tyr 850 <210> SEQ ID NO 52 <211> LENGTH: 297 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 125 <400> SEQUENCE: 52 Met Ser Glu Leu Asn Ala Leu Leu Lys Asp Ile Asn Gly Ser Leu Thr 1 5 10 15 Ala Thr Ser Glu Ser Leu Glu Arg Leu Ser Gly Ile Tyr Ser Asn Ser 20 25 30 Ala Thr Asp Glu Ile Pro Glu Ser Asn Gln Leu His Glu His Leu Phe 35 40 45 Tyr Asp Ala Lys Lys Pro Ala Glu Lys Val Ser Leu Leu Ser Leu Lys 50 55 60 Asn Gly Ser Met Leu Gly Tyr Ile Asn Ser Leu Leu Met Leu Ile Gly 65 70 75 80 Asn Arg Leu Asp Asp Glu Cys Lys Asp Pro Ser Ala Met Asp Ala Arg 85 90 95 Glu Arg Ser Ile Gln His Arg Val Val Leu Glu Arg Gly Val Lys Pro 100 105 110 Leu Glu Lys Lys Leu Ala Tyr Gln Leu Asp Lys Leu Thr Arg Ala Tyr 115 120 125 Val Lys Met Glu Lys Glu Tyr Lys Asp Ala Glu Lys Arg Ala Leu Glu 130 135 140 Lys Ser Thr Leu Val Asn His Ser Gly Asn Asp Asp Ser Glu Asp Asp 145 150 155 160 Glu Ser Ser Glu Asp Glu Ile Ala Tyr Arg Pro Asn Thr Ser Gly Ile 165 170 175 Ile Asn Thr Asn Lys Lys Ser Ser Ala Tyr Arg Val Glu Glu Thr Ala 180 185 190 Lys Gln Glu Asn Gly Glu Glu Asn Asp Asp Asn Glu Thr Gly Val Tyr 195 200 205 Lys Pro Pro Lys Ile Thr Ala Val Leu Pro Pro Gln Gln Thr His Phe 210 215 220 Glu Asp Arg Phe Asp Ala Arg Glu His Lys Asp Arg Ser Asn Lys Ser 225 230 235 240 Asn Lys Ala Glu Lys Arg Lys Gln Lys Gln Arg Glu Arg Asn Ala Arg 245 250 255 Met Asn Val Ile Gly Gly Glu Asp Phe Gly Ile Phe Ser Ser Lys Arg 260 265 270 Lys Leu Glu Asp Ser Thr Ser Arg Arg Gly Ala Lys Lys Thr Arg Ser 275 280 285 Ala Trp Asp Arg Ala Gln Arg Arg Leu 290 295 <210> SEQ ID NO 53 <211> LENGTH: 300 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 126 <400> SEQUENCE: 53 Met Ser Lys Val Asp Thr Val Leu Lys Glu Ile Ile Ser Ser Thr Lys 1 5 10 15 Ser Thr Glu Ala Ser Val Lys Glu Leu Ile Ala Phe Val Lys Asp Ser 20 25 30 Ser Ser Gln His Pro Glu Leu Val Arg Asn Leu Leu Ala Lys Ser Asn 35 40 45 Ser Ser Leu Glu Gly Val Ser Leu Leu Gly Leu Lys Asn Glu Ser Leu 50 55 60 Val Ser Tyr Ile Asn Asn Ile Val Leu Val Val Leu Ser His Leu Glu 65 70 75 80 Arg Leu Glu Ser Asp Ser Glu Thr Gly Ser Ser Ala Val Glu Arg Ser 85 90 95 Ile Ile Gln Arg Val Thr Leu Glu Lys Gly Val Lys Pro Leu Glu Lys 100 105 110 Lys Leu Ser Tyr Gln Leu Asp Lys Met Ile Arg Ala Tyr Gly Arg Met 115 120 125 Glu Gln Asp Glu Ile Lys Ala Glu Gln Lys Leu Asn Asp Arg Gly Ser 130 135 140 Gly Glu Asn Asp Glu Asn Asp Glu Asn Asp Ser Glu Glu Asp Ser Glu 145 150 155 160 Glu Asp Ser Glu Asp Asp Ser Glu Asp Asp Glu Leu Ala Tyr Arg Pro 165 170 175 Asp Ala Ser Ser Phe Ala Lys Leu Thr Ser Ala Lys Thr Lys Ser Lys 180 185 190 Pro Thr Ser Ser Ala Val Ser Thr Ser Asn Glu Lys Tyr Arg Pro Pro 195 200 205 Lys Ile Ser Ala Met Ala Pro Pro Thr Ala Val Lys Ser His Asp Leu 210 215 220 Asp Ala Asn Thr Thr Ser Ser Lys Asn Arg Lys Leu Gln Ser Met Glu 225 230 235 240 Glu Tyr Leu Gln Glu Gln Ser Asp Met Pro Met Val Glu Ala Ser Val 245 250 255 Gly Ser Thr Ile Val Glu His Gly Arg Gly Gly Val Lys Thr Gln His 260 265 270 Asp Arg Lys Lys Glu Arg Glu Ile Gln Thr Tyr Glu Glu Asp Asn Phe 275 280 285 Val Arg Leu Pro Thr Ser Gln Thr Lys Lys Ser Phe 290 295 300 <210> SEQ ID NO 54 <211> LENGTH: 311 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 127 <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/AL050003 <309> DATABASE ENTRY DATE: 2000-02-18 <313> RELEVANT RESIDUES: (1)..(311) <400> SEQUENCE: 54 Met Ala Ala Leu Gly Val Leu Glu Ser Asp Leu Pro Ser Ala Val Thr 1 5 10 15 Leu Leu Lys Asn Leu Gln Glu Gln Val Met Ala Val Thr Ala Gln Val 20 25 30 Lys Ser Leu Thr Gln Lys Val Gln Ala Gly Ala Tyr Pro Thr Glu Lys 35 40 45 Gly Leu Ser Phe Leu Glu Val Lys Asp Gln Leu Leu Leu Met Tyr Leu 50 55 60 Met Asp Leu Thr His Leu Ile Leu Asp Lys Ala Ser Gly Gly Ser Leu 65 70 75 80 Gln Gly His Asp Ala Val Leu Arg Leu Val Glu Ile Arg Thr Val Leu 85 90 95 Glu Lys Leu Arg Pro Leu Asp Gln Lys Leu Lys Tyr Gln Ile Asp Lys 100 105 110 Leu Ile Lys Thr Ala Val Thr Gly Ser Leu Ser Glu Asn Asp Pro Leu 115 120 125 Arg Phe Lys Pro His Pro Ser Asn Met Met Ser Lys Leu Ser Ser Glu 130 135 140 Asp Glu Glu Glu Asp Glu Ala Glu Asp Asp Gln Ser Glu Ala Ser Gly 145 150 155 160 Lys Lys Ser Val Lys Gly Val Ser Lys Lys Tyr Val Pro Pro Arg Leu 165 170 175 Val Pro Val His Tyr Asp Glu Thr Glu Ala Glu Arg Glu Lys Lys Arg 180 185 190 Leu Glu Arg Ala Lys Arg Arg Ala Leu Ser Ser Ser Val Ile Arg Glu 195 200 205 Leu Lys Glu Gln Tyr Ser Asp Ala Pro Glu Glu Ile Arg Asp Ala Arg 210 215 220 His Pro His Val Thr Arg Gln Ser Gln Glu Asp Gln His Arg Ile Asn 225 230 235 240 Tyr Glu Glu Ser Met Met Val Arg Leu Ser Val Ser Lys Arg Glu Lys 245 250 255 Gly Arg Arg Lys Arg Ala Asn Val Met Ser Ser Gln Leu His Ser Leu 260 265 270 Thr His Phe Ser Asp Ile Ser Ala Leu Thr Gly Gly Thr Val His Leu 275 280 285 Asp Glu Asp Gln Asn Pro Ile Lys Lys Arg Lys Lys Ile Pro Gln Lys 290 295 300 Gly Arg Lys Lys Lys Gly Gln 305 310 <210> SEQ ID NO 55 <211> LENGTH: 221 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 128 <400> SEQUENCE: 55 Met Ser Ala Thr Glu Ser Ser Ser Ile Phe Thr Leu Ser His Asn Ser 1 5 10 15 Asn Leu Gln Asp Ile Leu Ala Ala Asn Ala Lys Trp Ala Ser Gln Met 20 25 30 Asn Asn Ile Gln Pro Thr Leu Phe Pro Asp His Asn Ala Lys Gly Gln 35 40 45 Ser Pro His Thr Leu Phe Ile Gly Cys Ser Asp Ser Arg Tyr Asn Glu 50 55 60 Asn Cys Leu Gly Val Leu Pro Gly Glu Val Phe Thr Trp Lys Asn Val 65 70 75 80 Ala Asn Ile Cys His Ser Glu Asp Leu Thr Leu Lys Ala Thr Leu Glu 85 90 95 Phe Ala Ile Ile Cys Leu Lys Val Asn Lys Val Ile Ile Cys Gly His 100 105 110 Thr Asp Cys Gly Gly Ile Lys Thr Cys Leu Thr Asn Gln Arg Glu Ala 115 120 125 Leu Pro Lys Val Asn Cys Ser His Leu Tyr Lys Tyr Leu Asp Asp Ile 130 135 140 Asp Thr Met Tyr His Glu Glu Ser Gln Asn Leu Ile His Leu Lys Thr 145 150 155 160 Gln Arg Glu Lys Ser His Tyr Leu Ser His Cys Asn Val Lys Arg Gln 165 170 175 Phe Asn Arg Ile Ile Glu Asn Pro Thr Val Gln Thr Ala Val Gln Asn 180 185 190 Gly Glu Leu Gln Val Tyr Gly Leu Leu Tyr Asn Val Glu Asp Gly Leu 195 200 205 Leu Gln Thr Val Ser Thr Tyr Thr Lys Val Thr Pro Lys 210 215 220 <210> SEQ ID NO 56 <211> LENGTH: 281 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 129 <400> SEQUENCE: 56 Met Gly Arg Glu Asn Ile Leu Lys Tyr Gln Leu Glu His Asp His Glu 1 5 10 15 Ser Asp Leu Val Thr Glu Lys Asp Gln Ser Leu Leu Leu Asp Asn Asn 20 25 30 Asn Asn Leu Asn Gly Met Asn Asn Thr Ile Lys Thr His Pro Val Arg 35 40 45 Val Ser Ser Gly Asn His Asn Asn Phe Pro Phe Thr Leu Ser Ser Glu 50 55 60 Ser Thr Leu Gln Asp Phe Leu Asn Asn Asn Lys Phe Phe Val Asp Ser 65 70 75 80 Ile Lys His Asn His Gly Asn Gln Ile Phe Asp Leu Asn Gly Gln Gly 85 90 95 Gln Ser Pro His Thr Leu Trp Ile Gly Cys Ser Asp Ser Arg Ala Gly 100 105 110 Asp Gln Cys Leu Ala Thr Leu Pro Gly Glu Ile Phe Val His Arg Asn 115 120 125 Ile Ala Asn Ile Val Asn Ala Asn Asp Ile Ser Ser Gln Gly Val Ile 130 135 140 Gln Phe Ala Ile Asp Val Leu Lys Val Lys Lys Ile Ile Val Cys Gly 145 150 155 160 His Thr Asp Cys Gly Gly Ile Trp Ala Ser Leu Ser Lys Lys Lys Ile 165 170 175 Gly Gly Val Leu Asp Leu Trp Leu Asn Pro Val Arg His Ile Arg Ala 180 185 190 Ala Asn Leu Lys Leu Leu Glu Glu Tyr Asn Gln Asp Pro Lys Leu Lys 195 200 205 Ala Lys Lys Leu Ala Glu Leu Asn Val Ile Ser Ser Val Thr Ala Leu 210 215 220 Lys Arg His Pro Ser Ala Ser Val Ala Leu Lys Lys Asn Glu Ile Glu 225 230 235 240 Val Trp Gly Met Leu Tyr Asp Val Ala Thr Gly Tyr Leu Ser Gln Val 245 250 255 Glu Ile Pro Gln Asp Glu Phe Glu Asp Leu Phe His Val His Asp Glu 260 265 270 His Asp Glu Glu Glu Tyr Asn Pro His 275 280 <210> SEQ ID NO 57 <211> LENGTH: 281 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 130 <400> SEQUENCE: 57 Met Lys Ala Arg Lys Ser Gln Arg Lys Ala Gly Ser Lys Pro Asn Leu 1 5 10 15 Ile Gln Ser Lys Leu Gln Val Asn Asn Gly Ser Lys Ser Asn Lys Ile 20 25 30 Val Lys Cys Asp Lys Cys Glu Met Ser Tyr Ser Ser Thr Ser Ile Glu 35 40 45 Asp Arg Ala Ile His Glu Lys Tyr His Thr Leu Gln Leu His Gly Arg 50 55 60 Lys Trp Ser Pro Asn Trp Gly Ser Ile Val Tyr Thr Glu Arg Asn His 65 70 75 80 Ser Arg Thr Val His Leu Ser Arg Ser Thr Gly Thr Ile Thr Pro Leu 85 90 95 Asn Ser Ser Pro Leu Lys Lys Ser Ser Pro Ser Ile Thr His Gln Glu 100 105 110 Glu Lys Ile Val Tyr Val Arg Pro Asp Lys Ser Asn Gly Glu Val Arg 115 120 125 Ala Met Thr Glu Ile Met Thr Leu Val Asn Asn Glu Leu Asn Ala Pro 130 135 140 His Asp Glu Asn Val Ile Trp Asn Ser Thr Thr Glu Glu Lys Gly Lys 145 150 155 160 Ala Phe Val Tyr Ile Arg Asn Asp Arg Ala Val Gly Ile Ile Ile Ile 165 170 175 Glu Asn Leu Tyr Gly Gly Asn Gly Lys Thr Ser Ser Arg Gly Arg Trp 180 185 190 Met Val Tyr Asp Ser Arg Arg Leu Val Gln Asn Val Tyr Pro Asp Phe 195 200 205 Lys Ile Gly Ile Ser Arg Ile Trp Val Cys Arg Thr Ala Arg Lys Leu 210 215 220 Gly Ile Ala Thr Lys Leu Ile Asp Val Ala Arg Glu Asn Ile Val Tyr 225 230 235 240 Gly Glu Val Ile Pro Arg Tyr Gln Val Ala Trp Ser Gln Pro Thr Asp 245 250 255 Ser Gly Gly Lys Leu Ala Ser Lys Tyr Asn Gly Ile Met His Lys Ser 260 265 270 Gly Lys Leu Leu Leu Pro Val Tyr Ile 275 280 <210> SEQ ID NO 58 <211> LENGTH: 260 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 131 <400> SEQUENCE: 58 Met Gly Ser Ile Asn Ser Gln Lys Ala Gln Lys Ile Gln Ser Ile Leu 1 5 10 15 Ala Leu Pro Ser Asn Phe Lys Lys Ile Thr Cys Ser Thr Cys Asp Met 20 25 30 Thr Tyr Asn Pro His Ile Ser Gln Asp Lys Leu Leu His Asn Lys Tyr 35 40 45 His Thr Asn Phe Ile Asn Gly Ile Pro Trp Asn Tyr Lys Thr Asp Asn 50 55 60 Asp Val Leu Ile Ile Glu Asn Phe Thr Leu Val Glu Thr Pro Lys Leu 65 70 75 80 Asn Ser Thr Gly Lys Ser Leu Lys Leu Thr Lys Thr Arg Gln Thr Phe 85 90 95 Lys Gly Ser Ile Ile Cys Ile Asn Lys Ser Asn Lys Arg His Ile Gln 100 105 110 Lys Val Glu Leu Leu Leu Asn Met Val Asn Gln Glu Leu Asn Ala Ser 115 120 125 Gln Asp Ser Gly Gln Trp Lys Lys Pro Glu Phe Asp Arg Ser Lys Ala 130 135 140 Phe Val Ile Ile Ile Asp Ser Lys Ala Ile Gly Leu Cys Thr Thr Asp 145 150 155 160 Thr Ile Gln Pro Asp Gln Gly Arg Trp Met Ile His Lys Thr Gln Ser 165 170 175 Ile Val Pro Asn Gln Ile Asn Lys Asn Val Val Ile Gly Ile Ser Arg 180 185 190 Ile Trp Ile Ser Arg Lys Trp Arg Gln Tyr Gly Leu Gly Lys Lys Leu 195 200 205 Leu Asn Val Val Leu Lys Asn Ser Ile Tyr Ser Val Gln Leu Leu Lys 210 215 220 Asn Gln Val Ala Phe Ser Gln Pro Ser Phe Ser Gly Gly Met Leu Ala 225 230 235 240 Lys Ser Phe Asn Gly Val Lys His Lys Ser Gly Glu Met Leu Leu Pro 245 250 255 Val Tyr Ile Glu 260 <210> SEQ ID NO 59 <211> LENGTH: 620 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 132 <400> SEQUENCE: 59 Met Leu Asn Gly Glu Asp Phe Val Glu His Asn Asp Ile Leu Ser Ser 1 5 10 15 Pro Ala Lys Ser Arg Asn Val Thr Pro Lys Arg Val Asp Pro His Gly 20 25 30 Glu Arg Gln Leu Arg Arg Ile His Ser Ser Lys Lys Asn Leu Leu Glu 35 40 45 Arg Ile Ser Leu Val Gly Asn Glu Arg Lys Asn Thr Ser Pro Asp Pro 50 55 60 Ala Leu Lys Pro Lys Thr Pro Ser Lys Ala Pro Arg Lys Arg Gly Arg 65 70 75 80 Pro Arg Lys Ile Gln Glu Glu Leu Thr Asp Arg Ile Lys Lys Asp Glu 85 90 95 Lys Asp Thr Ile Ser Ser Lys Lys Lys Arg Lys Leu Asp Lys Asp Thr 100 105 110 Ser Gly Asn Val Asn Glu Glu Ser Lys Thr Ser Asn Asn Lys Gln Val 115 120 125 Met Glu Lys Thr Gly Ile Lys Glu Lys Arg Glu Arg Glu Lys Ile Gln 130 135 140 Val Ala Thr Thr Thr Tyr Glu Asp Asn Val Thr Pro Gln Thr Asp Asp 145 150 155 160 Asn Phe Val Ser Asn Ser Pro Glu Pro Pro Glu Pro Ala Thr Pro Ser 165 170 175 Lys Lys Ser Leu Thr Thr Asn His Asp Phe Thr Ser Pro Leu Lys Gln 180 185 190 Ile Ile Met Asn Asn Leu Lys Glu Tyr Lys Asp Ser Thr Ser Pro Gly 195 200 205 Lys Leu Thr Leu Ser Arg Asn Phe Thr Pro Thr Pro Val Pro Lys Asn 210 215 220 Lys Lys Leu Tyr Gln Thr Ser Glu Thr Lys Ser Ala Ser Ser Phe Leu 225 230 235 240 Asp Thr Phe Glu Gly Tyr Phe Asp Gln Arg Lys Ile Val Arg Thr Asn 245 250 255 Ala Lys Ser Arg His Thr Met Ser Met Ala Pro Asp Val Thr Arg Glu 260 265 270 Glu Phe Ser Leu Val Ser Asn Phe Phe Asn Glu Asn Phe Gln Lys Arg 275 280 285 Pro Arg Gln Lys Leu Phe Glu Ile Gln Lys Lys Met Phe Pro Gln Tyr 290 295 300 Trp Phe Glu Leu Thr Gln Gly Phe Ser Leu Leu Phe Tyr Gly Val Gly 305 310 315 320 Ser Lys Arg Asn Phe Leu Glu Glu Phe Ala Ile Asp Tyr Leu Ser Pro 325 330 335 Lys Ile Ala Tyr Ser Gln Leu Ala Tyr Glu Asn Glu Leu Gln Gln Asn 340 345 350 Lys Pro Val Asn Ser Ile Pro Cys Leu Ile Leu Asn Gly Tyr Asn Pro 355 360 365 Ser Cys Asn Tyr Arg Asp Val Phe Lys Glu Ile Thr Asp Leu Leu Val 370 375 380 Pro Ala Glu Leu Thr Arg Ser Glu Thr Lys Tyr Trp Gly Asn His Val 385 390 395 400 Ile Leu Gln Ile Gln Lys Met Ile Asp Phe Tyr Lys Asn Gln Pro Leu 405 410 415 Asp Ile Lys Leu Ile Leu Val Val His Asn Leu Asp Gly Pro Ser Ile 420 425 430 Arg Lys Asn Thr Phe Gln Thr Met Leu Ser Phe Leu Ser Val Ile Arg 435 440 445 Gln Ile Ala Ile Val Ala Ser Thr Asp His Ile Tyr Ala Pro Leu Leu 450 455 460 Trp Asp Asn Met Lys Ala Gln Asn Tyr Asn Phe Val Phe His Asp Ile 465 470 475 480 Ser Asn Phe Glu Pro Ser Thr Val Glu Ser Thr Phe Gln Asp Val Met 485 490 495 Lys Met Gly Lys Ser Asp Thr Ser Ser Gly Ala Glu Gly Ala Lys Tyr 500 505 510 Val Leu Gln Ser Leu Thr Val Asn Ser Lys Lys Met Tyr Lys Leu Leu 515 520 525 Ile Glu Thr Gln Met Gln Asn Met Gly Asn Leu Ser Ala Asn Thr Gly 530 535 540 Pro Lys Arg Gly Thr Gln Arg Thr Gly Val Glu Leu Lys Leu Phe Asn 545 550 555 560 His Leu Cys Ala Ala Asp Phe Ile Ala Ser Asn Glu Ile Ala Leu Arg 565 570 575 Ser Met Leu Arg Glu Phe Ile Glu His Lys Met Ala Asn Ile Thr Lys 580 585 590 Asn Asn Ser Gly Met Glu Ile Ile Trp Val Pro Tyr Thr Tyr Ala Glu 595 600 605 Leu Glu Lys Leu Leu Lys Thr Val Leu Asn Thr Leu 610 615 620 <210> SEQ ID NO 60 <211> LENGTH: 600 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 133 <400> SEQUENCE: 60 Met Ser His Ser Asn Ala Leu Pro Asn Ser Pro Phe Arg Ser Pro Lys 1 5 10 15 Lys Gln Arg Met Glu Val Ile Gly Pro Leu Asn Ala Ser Arg Phe Ser 20 25 30 Phe Ser Pro Val Lys Thr Pro Pro His Gly Arg Ala Gly Leu Ser Ser 35 40 45 Pro Glu Lys Arg Leu Val Lys Asp Leu Asp Lys Ala Arg Lys Arg Ala 50 55 60 Asn Asn Ser Leu Tyr Asn Arg Leu Met Asp Glu Tyr Leu Asp Thr Asp 65 70 75 80 Asp Tyr Leu Asp Glu Gln Asp Arg Ile Leu Ala Asp Arg Ile Ile Lys 85 90 95 Gln Ser Arg Gly Glu Pro Asp Glu Val Asn Tyr Gly Ser Asp Val Glu 100 105 110 Leu Glu Ile Asp Leu Thr Gln Gln Arg Arg Thr Arg Arg Arg Glu Lys 115 120 125 Lys Val Val Tyr Ser Ser Asp Ser Ser Asn Glu Tyr Glu Asp Thr Gly 130 135 140 Met Pro Glu Glu Ser Ser Ser Glu Glu Glu Glu Ala Asp Asp Asp Asp 145 150 155 160 Gly Asn Val Glu Phe Val Tyr Gly Pro Pro Lys Glu Arg Lys Thr Ser 165 170 175 Leu Ser Ser Ser Pro Pro Thr Val Lys Pro Thr Val Arg Arg Thr Lys 180 185 190 Arg Gly Arg Pro Ser Lys Ser Glu Leu Val Leu Gly Gln Ile Lys Ser 195 200 205 Ile Phe His Gln Asp Asp Val Leu Phe Ser Thr Asp Arg Lys Thr Phe 210 215 220 Thr Pro Thr Lys Pro Thr Ala Ala Lys Lys Pro Val Ser Asn Tyr Leu 225 230 235 240 Thr Ser Ile Phe Asp Gln Asn Phe Asp Arg Ser Lys Val Pro Ser Leu 245 250 255 Ser Gly Ile Pro Lys Ser Thr Asn Thr His Glu Glu Lys Lys Thr Phe 260 265 270 Val Pro Leu Pro Ile Pro Thr Leu Asp Ala Asp Gly Asn Ile Thr Asp 275 280 285 Lys Glu Tyr Ile Ser Lys Tyr Phe Asp Gly Val Asp Pro Ala Lys Phe 290 295 300 Lys Glu Gly Arg Phe Val Asp Glu Lys Val Phe Tyr Leu Glu Gly Pro 305 310 315 320 Glu Gly Tyr Phe Glu Gln Gln Thr Thr Arg Val Lys Gln Ser Gly Asn 325 330 335 Ser Leu Thr Ala Leu Ala Pro Gln Ile Glu Tyr Lys Asp Phe Ala Arg 340 345 350 Leu Val Lys Leu Gly Asp Asn Leu Ser Phe Gln Arg Lys Arg His Leu 355 360 365 Phe Glu Leu His Lys Tyr Ile Tyr His Gln Trp Cys Phe Glu Met Ser 370 375 380 Gln Gly Phe Asn Leu Asn Phe Tyr Gly Val Gly Ser Lys Ile Asp Leu 385 390 395 400 Leu Arg Asp Phe Ala Thr Asn Tyr Phe Gly Ile Trp Trp Glu Asn Val 405 410 415 Val His Ala Asp Leu Pro Lys Val Leu Val Val Asn Gly Phe Asn Pro 420 425 430 Ser Ile Asn Ile Lys Lys Leu Ile Leu Glu Ile Ala Ser Ile Leu Leu 435 440 445 Pro Asn Glu Leu Tyr Pro Lys His Ile Ala Gly Thr Val Pro Phe Val 450 455 460 Val Asp Tyr Leu Asn Asn His Arg Leu Pro Cys Gly Ser Ile Gly Phe 465 470 475 480 His Lys Pro Lys Ile Leu Leu Ile Ile His Asn Leu Asp Gly Glu Val 485 490 495 Phe Arg Val Asp Lys Thr Gln Thr Leu Leu Ser Gln Leu Met Thr Leu 500 505 510 Pro Glu Val Trp Ala Met Ser Ser Thr Asp His Ile Asn Ala Ser Leu 515 520 525 Leu Trp Asp Leu Ser Lys Val Lys Asn Leu Asn Phe Ile Trp His Asn 530 535 540 Leu Thr Thr Tyr Ala Thr Tyr Gln Arg Glu Thr Ser Phe Arg Asp Val 545 550 555 560 Ile Ser Leu Gly Lys Ser Lys Lys Phe Val Gly Gly Leu Gly Ala Lys 565 570 575 Tyr Val Leu Arg Ser Leu Thr Asp Asn His Arg Asn Leu Tyr Arg Glu 580 585 590 Leu Leu Ile Ala Gln Leu Asp Lys 595 600 <210> SEQ ID NO 61 <211> LENGTH: 577 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 134 <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/Q13416 <309> DATABASE ENTRY DATE: 2000-05-30 <313> RELEVANT RESIDUES: (1)..(577) <400> SEQUENCE: 61 Met Ser Lys Pro Glu Leu Lys Glu Asp Lys Met Leu Glu Val His Phe 1 5 10 15 Val Gly Asp Asp Asp Val Leu Asn His Ile Leu Asp Arg Glu Gly Gly 20 25 30 Ala Lys Leu Lys Lys Glu Arg Ala Gln Leu Leu Val Asn Pro Lys Lys 35 40 45 Ile Ile Lys Lys Pro Glu Tyr Asp Leu Glu Glu Asp Asp Gln Glu Val 50 55 60 Leu Lys Asp Gln Asn Tyr Val Glu Ile Met Gly Arg Asp Val Gln Glu 65 70 75 80 Ser Leu Lys Asn Gly Ser Ala Thr Gly Gly Gly Asn Lys Val Tyr Ser 85 90 95 Phe Gln Asn Arg Lys His Ser Glu Lys Met Ala Lys Leu Ala Ser Glu 100 105 110 Leu Ala Lys Thr Pro Gln Lys Ser Val Ser Phe Ser Leu Lys Asn Asp 115 120 125 Pro Glu Ile Thr Ile Asn Val Pro Gln Ser Ser Lys Gly His Ser Ala 130 135 140 Ser Asp Lys Val Gln Pro Lys Asn Asn Asp Lys Ser Glu Phe Leu Ser 145 150 155 160 Thr Ala Pro Arg Ser Leu Arg Lys Arg Leu Ile Val Pro Arg Ser His 165 170 175 Ser Asp Ser Glu Ser Glu Tyr Ser Ala Ser Asn Ser Glu Asp Asp Glu 180 185 190 Gly Val Ala Gln Glu His Glu Glu Asp Thr Asn Ala Val Ile Phe Ser 195 200 205 Gln Lys Ile Gln Ala Gln Asn Arg Val Val Ser Ala Pro Val Gly Lys 210 215 220 Glu Thr Pro Ser Lys Arg Met Lys Arg Asp Lys Thr Ser Asp Leu Val 225 230 235 240 Glu Glu Tyr Phe Glu Ala His Ser Ser Ser Lys Val Leu Thr Ser Asp 245 250 255 Arg Thr Leu Gln Lys Leu Lys Arg Ala Lys Leu Asp Gln Gln Thr Leu 260 265 270 Arg Asn Leu Leu Ser Lys Val Ser Pro Ser Phe Ser Ala Glu Leu Lys 275 280 285 Gln Leu Asn Gln Gln Tyr Glu Lys Leu Phe His Lys Trp Met Leu Gln 290 295 300 Leu His Leu Gly Phe Asn Ile Val Leu Tyr Gly Leu Gly Ser Lys Arg 305 310 315 320 Asp Leu Leu Glu Arg Phe Arg Thr Thr Met Leu Gln Asp Ser Ile His 325 330 335 Val Val Ile Asn Gly Phe Phe Pro Gly Ile Ser Val Lys Ser Val Leu 340 345 350 Asn Ser Ile Thr Glu Glu Val Leu Asp His Met Gly Thr Phe Arg Ser 355 360 365 Ile Leu Asp Gln Leu Asp Trp Ile Val Asn Lys Phe Lys Glu Asp Ser 370 375 380 Ser Leu Glu Leu Phe Leu Leu Ile His Asn Leu Asp Ser Gln Met Leu 385 390 395 400 Arg Gly Glu Lys Ser Gln Gln Ile Ile Gly Gln Leu Ser Ser Leu His 405 410 415 Asn Ile Tyr Leu Ile Ala Ser Ile Asp His Leu Asn Ala Pro Leu Met 420 425 430 Trp Asp His Ala Lys Gln Ser Leu Phe Asn Trp Leu Trp Tyr Glu Thr 435 440 445 Thr Thr Tyr Ser Pro Tyr Thr Glu Glu Thr Ser Tyr Glu Asn Ser Leu 450 455 460 Leu Val Lys Gln Ser Gly Ser Leu Pro Leu Ser Ser Leu Thr His Val 465 470 475 480 Leu Arg Ser Leu Thr Pro Asn Ala Arg Gly Ile Phe Arg Leu Leu Ile 485 490 495 Lys Tyr Gln Leu Asp Asn Gln Asp Asn Pro Ser Tyr Ile Gly Leu Ser 500 505 510 Phe Gln Asp Phe Tyr Gln Gln Cys Arg Glu Ala Phe Leu Val Asn Ser 515 520 525 Asp Leu Thr Leu Arg Ala Gln Leu Thr Glu Phe Arg Asp His Lys Leu 530 535 540 Ile Arg Thr Lys Lys Gly Thr Asp Gly Val Glu Tyr Leu Leu Ile Pro 545 550 555 560 Val Asp Asn Gly Thr Leu Thr Asp Phe Leu Glu Lys Glu Glu Glu Glu 565 570 575 Ala <210> SEQ ID NO 62 <211> LENGTH: 385 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 135 <400> SEQUENCE: 62 Met Ser Ser Val Asn Ala Asn Gly Gly Tyr Thr Lys Pro Gln Lys Tyr 1 5 10 15 Val Pro Gly Pro Gly Asp Pro Glu Leu Pro Pro Gln Leu Ser Glu Phe 20 25 30 Lys Asp Lys Thr Ser Asp Glu Ile Leu Lys Glu Met Asn Arg Met Pro 35 40 45 Phe Phe Met Thr Lys Leu Asp Glu Thr Asp Gly Ala Gly Gly Glu Asn 50 55 60 Val Glu Leu Glu Ala Leu Lys Ala Leu Ala Tyr Glu Gly Glu Pro His 65 70 75 80 Glu Ile Ala Glu Asn Phe Lys Lys Gln Gly Asn Glu Leu Tyr Lys Ala 85 90 95 Lys Arg Phe Lys Asp Ala Arg Glu Leu Tyr Ser Lys Gly Leu Ala Val 100 105 110 Glu Cys Glu Asp Lys Ser Ile Asn Glu Ser Leu Tyr Ala Asn Arg Ala 115 120 125 Ala Cys Glu Leu Glu Leu Lys Asn Tyr Arg Arg Cys Ile Glu Asp Cys 130 135 140 Ser Lys Ala Leu Thr Ile Asn Pro Lys Asn Val Lys Cys Tyr Tyr Arg 145 150 155 160 Thr Ser Lys Ala Phe Phe Gln Leu Asn Lys Leu Glu Glu Ala Lys Ser 165 170 175 Ala Ala Thr Phe Ala Asn Gln Arg Ile Asp Pro Glu Asn Lys Ser Ile 180 185 190 Leu Asn Met Leu Ser Val Ile Asp Arg Lys Glu Gln Glu Leu Lys Ala 195 200 205 Lys Glu Glu Lys Gln Gln Arg Glu Ala Gln Glu Arg Glu Asn Lys Lys 210 215 220 Ile Met Leu Glu Ser Ala Met Thr Leu Arg Asn Ile Thr Asn Ile Lys 225 230 235 240 Thr His Ser Pro Val Glu Leu Leu Asn Glu Gly Lys Ile Arg Leu Glu 245 250 255 Asp Pro Met Asp Phe Glu Ser Gln Leu Ile Tyr Pro Ala Leu Ile Met 260 265 270 Tyr Pro Thr Gln Asp Glu Phe Asp Phe Val Gly Glu Val Ser Glu Leu 275 280 285 Thr Thr Val Gln Glu Leu Val Asp Leu Val Leu Glu Gly Pro Gln Glu 290 295 300 Arg Phe Lys Lys Glu Gly Lys Glu Asn Phe Thr Pro Lys Lys Val Leu 305 310 315 320 Val Phe Met Glu Thr Lys Ala Gly Gly Leu Ile Lys Ala Gly Lys Lys 325 330 335 Leu Thr Phe His Asp Ile Leu Lys Lys Glu Ser Pro Asp Val Pro Leu 340 345 350 Phe Asp Asn Ala Leu Lys Ile Tyr Ile Val Pro Lys Val Glu Ser Glu 355 360 365 Gly Trp Ile Ser Lys Trp Asp Lys Gln Lys Ala Leu Glu Arg Arg Ser 370 375 380 Val 385 <210> SEQ ID NO 63 <211> LENGTH: 300 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 136 <400> SEQUENCE: 63 Met Ser Lys Ile Glu Pro Val Thr Glu Lys Glu Glu Glu Tyr Val Ser 1 5 10 15 Glu Trp Asp Arg Arg Arg Tyr Val Pro Lys Ala Gly Glu Pro Glu Leu 20 25 30 Pro Pro Gln Leu Ser Glu Phe Ser Asn Lys Thr Thr Asp Glu Val Ile 35 40 45 Glu Glu Leu Asn Arg Leu Pro Phe Phe Met Thr Leu Asp Glu Thr Asp 50 55 60 Gly Asp Gly Gly Glu Asn Val Asn Leu Glu Ala Leu Lys Ser Leu Ala 65 70 75 80 Tyr Glu Gly Asp Pro Asp Glu Ile Ala Ser Asn Phe Lys Asn Gln Gly 85 90 95 Asn Asn Cys Tyr Lys Phe Lys Lys Tyr Lys Asp Ala Ile Ile Phe Tyr 100 105 110 Thr Lys Gly Leu Glu Val Asn Cys Asp Val Asp Ala Ile Asn Ser Ala 115 120 125 Leu Tyr Leu Asn Arg Ala Ala Cys Asn Leu Glu Leu Lys Asn Tyr Arg 130 135 140 Arg Cys Ile Glu Asp Cys Lys Lys Val Leu Met Leu Asp Glu Lys Asn 145 150 155 160 Ile Lys Ala Cys Phe Arg Ser Gly Lys Ala Phe Phe Ala Ile Glu Lys 165 170 175 Tyr Asp Glu Ala Ile Lys Val Leu Glu Tyr Gly Leu Asn Ile Glu Pro 180 185 190 Glu Asn Lys Asp Leu Gln Lys Leu Leu Gln Gln Val Gln Lys Arg Gln 195 200 205 Glu Thr Leu Ala Gln Ile Lys Ala Lys Lys Ala Gln Glu Glu Glu Gln 210 215 220 Glu Arg Leu Lys Asn Ile Val Leu Glu Asn Ser Ile Lys Leu Arg His 225 230 235 240 Ile Glu Ile Val Lys Ser Ser Ser Pro Pro Glu Val Leu Lys Thr Ala 245 250 255 Lys Ile Arg Leu Glu Asp Pro Lys Asp Tyr Gln Ser Gln Leu Ile Phe 260 265 270 Pro Ala Met Ile Leu Tyr Pro Thr Thr Asp Glu Phe Asp Phe Ile Ala 275 280 285 Glu Ile Ser Glu Leu Thr Thr Pro Leu Glu Leu Leu 290 295 300 <210> SEQ ID NO 64 <211> LENGTH: 356 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 137 <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/NP_004614 <309> DATABASE ENTRY DATE: 2000-11-01 <313> RELEVANT RESIDUES: (1)..(356) <400> SEQUENCE: 64 Met Glu Gln Pro Gly Gln Asp Pro Thr Ser Asp Asp Val Met Asp Ser 1 5 10 15 Phe Leu Glu Lys Phe Gln Ser Gln Pro Tyr Arg Gly Gly Phe His Glu 20 25 30 Asp Gln Trp Glu Lys Glu Phe Glu Lys Val Pro Leu Phe Met Ser Arg 35 40 45 Ala Pro Ser Glu Ile Asp Pro Arg Glu Asn Pro Asp Leu Ala Cys Leu 50 55 60 Gln Ser Ile Ile Phe Asp Glu Glu Arg Ser Pro Glu Glu Gln Ala Lys 65 70 75 80 Thr Tyr Lys Asp Glu Gly Asn Asp Tyr Phe Lys Glu Lys Asp Tyr Lys 85 90 95 Lys Ala Val Ile Ser Tyr Thr Glu Gly Leu Lys Lys Lys Cys Ala Asp 100 105 110 Pro Asp Leu Asn Ala Val Leu Tyr Thr Asn Arg Ala Ala Ala Gln Tyr 115 120 125 Tyr Leu Gly Asn Phe Arg Ser Ala Leu Asn Asp Val Thr Ala Ala Arg 130 135 140 Lys Leu Lys Pro Cys His Leu Lys Ala Ile Ile Arg Gly Ala Leu Cys 145 150 155 160 His Leu Glu Leu Ile His Phe Ala Glu Ala Val Asn Trp Cys Asp Glu 165 170 175 Gly Leu Gln Ile Asp Ala Lys Glu Lys Lys Leu Leu Glu Met Arg Ala 180 185 190 Lys Ala Asp Lys Leu Lys Arg Ile Glu Gln Arg Asp Val Arg Lys Ala 195 200 205 Asn Leu Lys Glu Lys Lys Glu Arg Asn Gln Asn Glu Ala Leu Leu Gln 210 215 220 Ala Ile Lys Ala Arg Asn Ile Arg Leu Ser Glu Ala Ala Cys Glu Asp 225 230 235 240 Glu Asp Ser Ala Ser Glu Gly Leu Gly Glu Leu Phe Leu Asp Gly Leu 245 250 255 Ser Thr Glu Asn Pro His Gly Ala Arg Leu Ser Leu Asp Gly Gln Gly 260 265 270 Arg Leu Ser Trp Pro Val Leu Phe Leu Tyr Pro Glu Tyr Ala Gln Ser 275 280 285 Asp Phe Ile Ser Ala Phe His Glu Asp Ser Arg Phe Ile Asp His Leu 290 295 300 Met Val Met Phe Gly Glu Thr Pro Ser Trp Asp Leu Glu Gln Lys Tyr 305 310 315 320 Cys Leu Ile Ile Trp Arg Ser Thr Leu Arg Met Arg Thr Gly Gln Asn 325 330 335 Tyr Thr Gly Cys Leu Pro Arg Ala Pro Cys Tyr Arg Phe Tyr Ser Thr 340 345 350 Arg Gly Thr Leu 355 <210> SEQ ID NO 65 <211> LENGTH: 167 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 138 <400> SEQUENCE: 65 Met Ser Thr Ile Pro Ser Glu Ile Ile Asn Trp Thr Ile Leu Asn Glu 1 5 10 15 Ile Ile Ser Met Asp Asp Asp Asp Ser Asp Phe Ser Lys Gly Leu Ile 20 25 30 Ile Gln Phe Ile Asp Gln Ala Gln Thr Thr Phe Ala Gln Met Gln Arg 35 40 45 Gln Leu Asp Gly Glu Lys Asn Leu Thr Glu Leu Asp Asn Leu Gly His 50 55 60 Phe Leu Lys Gly Ser Ser Ala Ala Leu Gly Leu Gln Arg Ile Ala Trp 65 70 75 80 Val Cys Glu Arg Ile Gln Asn Leu Gly Arg Lys Met Glu His Phe Phe 85 90 95 Pro Asn Lys Thr Glu Leu Val Asn Thr Leu Ser Asp Lys Ser Ile Ile 100 105 110 Asn Gly Ile Asn Ile Asp Glu Asp Asp Glu Glu Ile Lys Ile Gln Val 115 120 125 Asp Asp Lys Asp Glu Asn Ser Ile Tyr Leu Ile Leu Ile Ala Lys Ala 130 135 140 Leu Asn Gln Ser Arg Leu Glu Phe Lys Leu Ala Arg Ile Glu Leu Ser 145 150 155 160 Lys Tyr Tyr Asn Thr Asn Leu 165 <210> SEQ ID NO 66 <211> LENGTH: 184 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 139 <400> SEQUENCE: 66 Met Ser Glu Asp Lys Leu Gln Lys Leu Gln Asp Ser Gly Leu Val Asp 1 5 10 15 Trp Ala Val Phe Ser Glu Ile Val Thr Met Asp Glu Asp Glu Glu Gly 20 25 30 Phe Ser Lys Ser Leu Val Glu Val Phe Val Ser Gln Val Glu Glu Thr 35 40 45 Phe Glu Glu Ile Asp Lys Tyr Leu Lys Glu Lys Asn Leu Glu Lys Leu 50 55 60 Ser Ser Ser Gly His Phe Leu Lys Gly Ser Ala Ala Ala Leu Gly Leu 65 70 75 80 Thr Lys Ile Ser Asn Gln Cys Glu Arg Ile Gln Asn Tyr Gly His Lys 85 90 95 Ile Asn Phe Asp Asn Phe Gln Leu Glu Asp Ile Lys Thr Lys Gly Asp 100 105 110 Ser Ala Val Ser Ala Glu Asn Val Ala Val Asn Asp Gly Glu Thr Asn 115 120 125 Pro Glu Asn Gly Ser Asn Gly Asn Glu Thr Ser Asn Asn Lys Thr Asn 130 135 140 Thr Ser Asn Ile Pro Asp Glu Ser Ser Asp Asp Phe Trp Ile Ala Leu 145 150 155 160 Ile Glu Asp Ala Leu Ala Lys Ala Arg Asp Gly Phe Asp Gln Ser Arg 165 170 175 Arg Ala Leu Asp Glu Tyr Tyr Glu 180 <210> SEQ ID NO 67 <211> LENGTH: 240 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 140 <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/CAA78727 <309> DATABASE ENTRY DATE: 1993-01-10 <313> RELEVANT RESIDUES: (1)..(240) <400> SEQUENCE: 67 Thr Asp Lys Leu Ser Asn Met Gln Lys Asp Leu Glu Asn Ser Asn Ala 1 5 10 15 Lys Leu Gln Glu Lys Ile Gln Glu Leu Lys Ala Asn Glu His Gln Leu 20 25 30 Ile Thr Leu Lys Lys Asp Val Asn Glu Thr Gln Lys Lys Val Ser Glu 35 40 45 Met Glu Gln Leu Lys Lys Gln Ile Lys Asp Gln Ser Leu Thr Leu Ser 50 55 60 Lys Leu Glu Ile Glu Asn Leu Asn Leu Ala Gln Glu Leu His Glu Asn 65 70 75 80 Leu Glu Glu Met Lys Ser Val Met Lys Glu Arg Asp Asn Leu Arg Arg 85 90 95 Val Glu Glu Thr Leu Lys Leu Glu Arg Asp Gln Leu Lys Glu Ser Leu 100 105 110 Gln Glu Thr Lys Ala Arg Asp Leu Glu Ile Gln Gln Glu Leu Lys Thr 115 120 125 Ala Arg Met Leu Ser Lys Glu His Lys Glu Thr Val Asp Lys Leu Arg 130 135 140 Glu Lys Ile Ser Glu Lys Thr Ile Gln Ile Ser Asp Ile Gln Lys Asp 145 150 155 160 Leu Asp Lys Ser Lys Asp Glu Leu Gln Lys Lys Ile Gln Glu Leu Gln 165 170 175 Lys Lys Glu Leu Gln Leu Leu Arg Val Lys Glu Asp Val Asn Met Ser 180 185 190 His Lys Lys Ile Asn Glu Met Glu Gln Leu Lys Lys Gln Phe Glu Pro 195 200 205 Asn Tyr Leu Cys Lys Cys Glu Met Asp Asn Phe Gln Leu Thr Lys Lys 210 215 220 Leu His Glu Ser Leu Glu Glu Ile Arg Ile Val Ala Lys Glu Arg Asp 225 230 235 240 <210> SEQ ID NO 68 <211> LENGTH: 93 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 141 <400> SEQUENCE: 68 Met Ser Phe Leu Gly Phe Gly Gly Gly Gln Pro Gln Leu Ser Ser Gln 1 5 10 15 Gln Lys Ile Gln Ala Ala Glu Ala Glu Leu Asp Leu Val Thr Asp Met 20 25 30 Phe Asn Lys Leu Val Asn Asn Cys Tyr Lys Lys Cys Ile Asn Thr Ser 35 40 45 Tyr Ser Glu Gly Glu Leu Asn Lys Asn Glu Ser Ser Cys Leu Asp Arg 50 55 60 Cys Val Ala Lys Tyr Phe Glu Thr Asn Val Gln Val Gly Glu Asn Met 65 70 75 80 Gln Lys Met Gly Gln Ser Phe Asn Ala Ala Gly Lys Phe 85 90 <210> SEQ ID NO 69 <211> LENGTH: 91 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 142 <400> SEQUENCE: 69 Met Phe Gly Leu Gly Gly Thr Thr Pro Gln Ile Ser Ser Gln Gln Lys 1 5 10 15 Leu Gln Ala Ala Glu Ala Glu Leu Asp Met Val Thr Gly Met Phe Asn 20 25 30 Ala Leu Val Ser Gln Cys His Thr Lys Cys Ile Asn Lys Ser Tyr Asn 35 40 45 Glu Ala Asp Ile Ser Lys Gln Glu Ser Leu Cys Leu Asp Arg Cys Val 50 55 60 Ala Lys Tyr Phe Glu Thr Asn Val Gln Val Gly Glu Asn Met Gln Lys 65 70 75 80 Leu Gly Gln Ser Gly Gln Phe Met Gly Arg Arg 85 90 <210> SEQ ID NO 70 <211> LENGTH: 90 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 143 <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/NP_036588 <309> DATABASE ENTRY DATE: 2001-12-19 <313> RELEVANT RESIDUES: (1)..(90) <400> SEQUENCE: 70 Met Asp Pro Leu Arg Ala Gln Gln Leu Ala Ala Glu Leu Glu Val Glu 1 5 10 15 Met Met Ala Asp Met Tyr Asn Arg Met Thr Ser Ala Cys His Arg Lys 20 25 30 Cys Val Pro Pro His Tyr Lys Glu Ala Glu Leu Ser Lys Gly Glu Ser 35 40 45 Val Cys Leu Asp Arg Cys Val Ser Lys Tyr Leu Asp Ile His Glu Arg 50 55 60 Met Gly Lys Lys Leu Thr Glu Leu Ser Met Gln Asp Glu Glu Leu Met 65 70 75 80 Lys Arg Val Gln Gln Ser Ser Gly Pro Ala 85 90 <210> SEQ ID NO 71 <211> LENGTH: 600 <212> TYPE: PRT <213> ORGANISM: Saccharomyces cerevisiae <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 144 <400> SEQUENCE: 71 Met Thr Thr Glu Asp Pro Asp Ser Asn His Leu Ser Ser Glu Thr Gly 1 5 10 15 Ile Lys Leu Ala Leu Asp Pro Asn Leu Ile Thr Leu Ala Leu Ser Ser 20 25 30 Asn Pro Asn Ser Ser Leu His Ser Pro Thr Ser Asp Glu Pro Val Pro 35 40 45 Glu Ser Ala Gly Lys Ala Asp Thr Ser Ile Arg Leu Glu Gly Asp Glu 50 55 60 Leu Glu Asn Lys Thr Lys Lys Asp Asn Asp Lys Asn Leu Lys Phe Leu 65 70 75 80 Lys Asn Lys Asp Ser Leu Val Ser Asn Pro His Glu Ile Tyr Gly Ser 85 90 95 Met Pro Leu Glu Gln Leu Ile Pro Ile Ile Leu Arg Gln Arg Gly Pro 100 105 110 Gly Phe Lys Phe Val Asp Leu Asn Glu Lys Glu Leu Gln Asn Glu Ile 115 120 125 Lys Gln Leu Gly Ser Asp Ser Ser Asp Gly His Asn Ser Glu Lys Lys 130 135 140 Asp Thr Asp Gly Ala Asp Glu Asn Val Gln Ile Gly Glu Asp Phe Met 145 150 155 160 Glu Val Asp Tyr Glu Asp Lys Asp Asn Pro Val Asp Ser Arg Asn Glu 165 170 175 Thr Asp His Lys Thr Asn Glu Asn Gly Glu Thr Asp Asp Asn Ile Glu 180 185 190 Thr Val Met Thr Gln Glu Gln Phe Val Lys Arg Arg Arg Asp Met Leu 195 200 205 Glu His Ile Asn Leu Ala Met Asn Glu Ser Ser Leu Ala Leu Glu Phe 210 215 220 Val Ser Leu Leu Leu Ser Ser Val Lys Glu Ser Thr Gly Met Ser Ser 225 230 235 240 Met Ser Pro Phe Leu Arg Lys Val Val Lys Pro Ser Ser Leu Asn Ser 245 250 255 Asp Lys Ile Pro Tyr Val Ala Pro Thr Lys Lys Glu Tyr Ile Glu Leu 260 265 270 Asp Ile Leu Asn Lys Gly Trp Lys Leu Gln Ser Leu Asn Glu Ser Lys 275 280 285 Asp Leu Leu Arg Ala Ser Phe Asn Lys Leu Ser Ser Ile Leu Gln Asn 290 295 300 Glu His Asp Tyr Trp Asn Lys Ile Met Gln Ser Ile Ser Asn Lys Asp 305 310 315 320 Val Ile Phe Lys Ile Arg Asp Arg Thr Ser Gly Gln Lys Leu Leu Ala 325 330 335 Ile Lys Tyr Gly Tyr Glu Asp Ser Gly Ser Thr Tyr Lys His Asp Arg 340 345 350 Gly Ile Ala Asn Ile Arg Asn Asn Ile Glu Ser Gln Asn Leu Asp Leu 355 360 365 Ile Pro His Ser Ser Ser Val Phe Lys Gly Thr Asp Phe Val His Ser 370 375 380 Val Lys Lys Phe Leu Arg Val Arg Ile Phe Thr Lys Ile Glu Ser Glu 385 390 395 400 Asp Asp Tyr Ile Leu Ser Gly Glu Ser Val Met Asp Arg Asp Ser Glu 405 410 415 Ser Glu Glu Ala Glu Thr Lys Asp Ile Arg Lys Gln Ile Gln Leu Leu 420 425 430 Lys Lys Ile Ile Phe Glu Lys Glu Leu Met Tyr Gln Ile Lys Lys Glu 435 440 445 Cys Ala Leu Leu Ile Ser Tyr Gly Val Ser Ile Glu Asn Glu Asn Lys 450 455 460 Val Ile Ile Glu Leu Pro Asn Glu Lys Phe Glu Ile Glu Leu Leu Ser 465 470 475 480 Leu Asp Asp Asp Ser Ile Val Asn His Glu Gln Asp Leu Pro Lys Ile 485 490 495 Asn Asp Lys Arg Ala Asn Leu Met Leu Val Met Leu Arg Leu Leu Leu 500 505 510 Val Val Ile Phe Lys Lys Thr Leu Arg Ser Arg Ile Ser Ser Pro His 515 520 525 Gly Leu Ile Asn Leu Asn Val Asp Asp Asp Ile Leu Ile Ile Arg Pro 530 535 540 Ile Leu Gly Lys Val Arg Phe Ala Asn Tyr Lys Leu Leu Leu Lys Lys 545 550 555 560 Ile Ile Lys Asp Tyr Val Leu Asp Ile Val Pro Gly Ser Ser Ile Thr 565 570 575 Glu Thr Glu Val Glu Arg Glu Gln Pro Gln Glu Asn Lys Asn Ile Asp 580 585 590 Asp Glu Asn Ile Thr Lys Leu Asn 595 600 <210> SEQ ID NO 72 <211> LENGTH: 587 <212> TYPE: PRT <213> ORGANISM: Candida albicans <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 145 <400> SEQUENCE: 72 Met Val Glu Lys Gln Phe Asn Ile Asp Leu Glu Leu Asn Asp Thr Gly 1 5 10 15 His Ile Asp Pro Phe Leu Gln Asp Glu Tyr Val Cys Phe Leu Thr Leu 20 25 30 Leu Val Phe Leu Val Leu Phe Phe Ser Leu Leu Thr Leu Pro Arg Asp 35 40 45 Lys Leu Lys Leu Glu Glu Leu Ile Pro Arg Ile Phe Glu Arg Lys Ser 50 55 60 Phe Leu Asn Val Thr Glu Asp Ser Leu Arg Lys Glu Ile Asp Asn Ser 65 70 75 80 Leu Lys Ile Ser Glu Glu Asp Ala Leu Asp Thr Glu Glu Ser Arg Glu 85 90 95 Asp Thr Val Glu Ala Asp Gln Gln Glu Val Phe Asn Lys His Lys Phe 100 105 110 Glu Leu Ser Lys Asn Ile Asn Asn Ala Leu Asn Glu Thr Gln Leu Ser 115 120 125 Leu Asp Phe Val Ser Leu Leu Ile Ser Ser Val Lys Pro Ser Leu Ala 130 135 140 Lys Ser Thr Ile Ser Pro His Leu Ser Lys Phe Val Lys Pro Thr Ser 145 150 155 160 Leu Asn Ser Asp Arg Leu Gly Gln Asp Ser Asn Asp Asn Gln Glu Ser 165 170 175 Lys Ala Thr Asp Ser Phe Gly Gln Gly Trp Lys Leu Glu Ser Leu Gly 180 185 190 Lys Ile Thr Asp Leu Phe Arg Glu Ala Ser Thr Asn Leu Asn Asp Gln 195 200 205 Val Ile Lys Glu Arg Arg Tyr Trp Asn Met Ile Asn Leu Val Leu Ala 210 215 220 Asn Asp Glu Val Leu Phe Arg Met Arg Asp Pro Gln Asn Asn Ala Arg 225 230 235 240 Ala Ile Gly Val Lys Tyr Gly Tyr Gly Asp Ser Gly Ser Asn Phe His 245 250 255 Asp Gln Gly Leu Ala Leu Leu Arg Lys Asp Asn Gln Thr Gly Glu Ile 260 265 270 Ser Phe His Pro Ile Ser Ser Ile Asn Asn Ala Lys Ile Val Glu Lys 275 280 285 Val Ser Arg Phe Ile Arg Val Lys Ile Leu Ser Gln Ile Asp Gly Asp 290 295 300 Tyr Met Leu Thr Gly Gln Ser Ile Phe Asn Phe Asp Phe Glu Lys Ser 305 310 315 320 Lys Gln Ser Ile Ile Asn Asp Ile Glu Lys Ala Arg Phe Phe Leu Phe 325 330 335 Glu Glu Asp Leu Phe His Gln Leu Ile Arg Glu Ala Lys Leu Leu Val 340 345 350 Asn Tyr Asn Val Ser Ile Ile Ser Asn Lys Ile Ile Ile Glu Ile Asn 355 360 365 Asn Ile Ile Ile Glu Ile Glu Ser Ile Val Tyr Asp Glu Leu Asn Glu 370 375 380 Glu Glu Leu Glu Asn Tyr Tyr Gln Asn Val Asn Glu Tyr Ser Thr Leu 385 390 395 400 His Asn Lys Lys Cys Gln Leu Ile Leu Asn Tyr Leu Lys Leu Met Leu 405 410 415 Cys Cys Tyr Tyr Lys Tyr Asn Leu Lys Leu Lys Gln Lys Val Pro Thr 420 425 430 Ala Leu Thr Lys Trp Lys Gln Ser Asn Ser His Pro Leu Ile Leu Arg 435 440 445 Pro Leu Val Gly Asn Met Arg His Glu Leu Asn Leu Leu Asn Met Lys 450 455 460 Ser Val Leu Asp Arg Leu Met His Ala His Glu Ser Glu Leu Ser Tyr 465 470 475 480 Ser Lys Leu Asp Val Glu Lys Phe Ile Asn Leu Ala Thr Arg Ser Lys 485 490 495 Lys Gln Asn Pro Phe Gln Lys Ser Ile Glu Lys Pro Ile Ser Lys Phe 500 505 510 His Leu Val Leu Cys Asn Lys Thr Ser Asn Met Leu Asp Val Asn Ile 515 520 525 Gln Leu Asp Asn Tyr Glu Leu Phe Val Asn Leu Ile Ile Asn Met Thr 530 535 540 Ile Ile Arg Phe Glu Thr Glu His Asp Phe Lys Asn Asn Val Asn Gly 545 550 555 560 Ile Asn Val Leu Gln Leu Gly Phe Ser Asp Phe Asn Glu Ile Glu Glu 565 570 575 Cys Leu Asp Trp Ser Ile Gln Asn Phe Val Leu 580 585 <210> SEQ ID NO 73 <211> LENGTH: 888 <212> TYPE: PRT <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <223> OTHER INFORMATION: Corresponds to SEQ ID NO: 146 <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/BAA88763 <309> DATABASE ENTRY DATE: 2000-01-06 <313> RELEVANT RESIDUES: (1)..(888) <400> SEQUENCE: 73 Met Tyr Gly Ser Ala Arg Ser Val Gly Lys Val Glu Pro Ser Ser Gln 1 5 10 15 Ser Pro Gly Arg Ser Pro Arg Leu Pro Arg Ser Pro Arg Leu Gly His 20 25 30 Arg Arg Thr Asn Ser Thr Gly Gly Ser Ser Gly Ser Ser Val Gly Gly 35 40 45 Gly Ser Gly Lys Thr Leu Ser Met Glu Asn Ile Gln Ser Leu Asn Ala 50 55 60 Ala Tyr Ala Thr Ser Gly Pro Met Tyr Leu Ser Asp His Glu Asn Val 65 70 75 80 Gly Ser Glu Thr Pro Lys Ser Thr Met Thr Leu Gly Arg Ser Gly Gly 85 90 95 Arg Leu Pro Tyr Gly Val Arg Met Thr Ala Met Gly Ser Ser Pro Asn 100 105 110 Ile Ala Ser Ser Gly Val Ala Ser Asp Thr Ile Ala Phe Gly Glu His 115 120 125 His Leu Pro Pro Val Ser Met Ala Ser Thr Val Pro His Ser Leu Arg 130 135 140 Gln Ala Arg Asp Asn Thr Ile Met Asp Leu Gln Thr Gln Leu Lys Glu 145 150 155 160 Val Leu Arg Glu Asn Asp Leu Leu Arg Lys Asp Val Glu Val Lys Glu 165 170 175 Ser Lys Leu Ser Ser Ser Met Asn Ser Ile Lys Thr Phe Trp Ser Pro 180 185 190 Glu Leu Lys Lys Glu Arg Ala Leu Arg Lys Asp Glu Ala Ser Lys Ile 195 200 205 Thr Ile Trp Lys Glu Gln Tyr Arg Val Val Gln Glu Glu Asn Gln His 210 215 220 Met Gln Met Thr Ile Gln Ala Leu Gln Asp Glu Leu Arg Ile Gln Arg 225 230 235 240 Asp Leu Asn Gln Leu Phe Gln Gln Asp Ser Ser Ser Arg Thr Gly Glu 245 250 255 Pro Cys Val Ala Glu Leu Thr Glu Glu Asn Phe Gln Arg Leu His Ala 260 265 270 Glu His Glu Arg Gln Ala Lys Glu Leu Phe Leu Leu Arg Lys Thr Leu 275 280 285 Glu Glu Met Glu Leu Arg Ile Glu Thr Gln Lys Gln Thr Leu Asn Ala 290 295 300 Arg Asp Glu Ser Ile Lys Lys Leu Leu Glu Met Leu Gln Ser Lys Gly 305 310 315 320 Leu Ser Ala Lys Ala Thr Glu Glu Asp His Glu Arg Thr Arg Arg Leu 325 330 335 Ala Glu Ala Glu Met His Val His His Leu Glu Ser Leu Leu Glu Gln 340 345 350 Lys Glu Lys Glu Asn Ser Met Leu Arg Glu Glu Met His Arg Arg Phe 355 360 365 Glu Asn Ala Pro Asp Ser Ala Lys Thr Lys Ala Leu Gln Thr Val Ile 370 375 380 Glu Met Lys Asp Ser Lys Ile Ser Ser Met Glu Arg Gly Leu Arg Asp 385 390 395 400 Leu Glu Glu Glu Ile Gln Met Leu Lys Ser Asn Gly Ala Leu Ser Thr 405 410 415 Glu Glu Arg Glu Glu Glu Met Lys Gln Met Glu Val Tyr Arg Ser His 420 425 430 Ser Lys Phe Met Lys Asn Lys Ile Gly Gln Val Lys Gln Glu Leu Ser 435 440 445 Arg Lys Asp Thr Glu Leu Leu Ala Leu Gln Thr Lys Leu Glu Thr Leu 450 455 460 Thr Asn Gln Phe Ser Asp Ser Lys Gln His Ile Glu Val Leu Lys Glu 465 470 475 480 Ser Leu Thr Ala Lys Glu Gln Arg Ala Ala Ile Leu Gln Thr Glu Val 485 490 495 Asp Ala Leu Arg Leu Arg Leu Glu Glu Lys Glu Thr Met Leu Asn Lys 500 505 510 Lys Thr Lys Gln Ile Gln Asp Met Ala Glu Glu Lys Gly Thr Gln Ala 515 520 525 Gly Glu Ile His Asp Leu Lys Asp Met Leu Asp Val Lys Glu Arg Lys 530 535 540 Val Asn Val Leu Gln Lys Lys Ile Glu Asn Leu Gln Glu Gln Leu Arg 545 550 555 560 Asp Lys Glu Lys Gln Met Ser Ser Leu Lys Glu Arg Val Lys Ser Leu 565 570 575 Gln Ala Asp Thr Thr Asn Thr Asp Thr Ala Leu Thr Thr Leu Glu Glu 580 585 590 Ala Leu Ala Glu Lys Glu Arg Thr Ile Glu Arg Leu Lys Glu Gln Arg 595 600 605 Asp Arg Asp Glu Arg Glu Lys Gln Glu Glu Ile Asp Asn Tyr Lys Lys 610 615 620 Asp Leu Lys Asp Leu Lys Glu Lys Val Ser Leu Leu Gln Gly Asp Leu 625 630 635 640 Ser Glu Lys Glu Ala Ser Leu Leu Asp Leu Lys Glu His Ala Ser Ser 645 650 655 Leu Ala Ser Ser Asp Glu Ser Ser Lys Ala Gln Ala Glu Val Asp Arg 660 665 670 Leu Leu Glu Ile Leu Lys Glu Val Glu Asn Glu Lys Asn Asp Lys Asp 675 680 685 Lys Lys Ile Ala Glu Leu Glu Ser Leu Thr Ser Arg Gln Val Lys Asp 690 695 700 Gln Asn Lys Lys Val Ala Asn Leu Lys His Lys Glu Gln Val Glu Lys 705 710 715 720 Lys Lys Ser Ala Gln Met Leu Glu Glu Ala Arg Arg Arg Glu Asp Asn 725 730 735 Leu Asn Asp Ser Ser Gln Gln Leu Gln Val Glu Glu Leu Leu Met Ala 740 745 750 Met Glu Lys Val Lys Gln Glu Leu Glu Ser Met Lys Ala Lys Leu Ser 755 760 765 Ser Thr Gln Gln Ser Leu Ala Glu Lys Glu Thr His Leu Thr Asn Leu 770 775 780 Arg Ala Glu Arg Arg Lys His Leu Glu Glu Val Leu Glu Met Lys Gln 785 790 795 800 Glu Ala Leu Leu Ala Ala Ile Ser Glu Lys Asp Ala Asn Ile Ala Leu 805 810 815 Leu Glu Leu Ser Ser Ser Lys Lys Lys Thr Gln Glu Glu Val Ala Ala 820 825 830 Leu Lys Arg Glu Lys Asp Arg Leu Val Gln Gln Leu Lys Gln Gln Thr 835 840 845 Gln Asn Arg Met Lys Leu Met Ala Asp Asn Tyr Glu Asp Asp His Phe 850 855 860 Lys Ser Ser His Ser Asn Gln Thr Asn His Lys Pro Ser Pro Asp Gln 865 870 875 880 Asp Glu Glu Glu Gly Ile Trp Ala 885 <210> SEQ ID NO 74 <211> LENGTH: 900 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/CAA96279.1 <309> DATABASE ENTRY DATE: 1997-08-11 <313> RELEVANT RESIDUES: (1)..(900) <400> SEQUENCE: 74 atgagtggaa tgatagaaaa tgggttacag ctatcggaca atgctaaaac cttacatagc 60 cagatgatgt cgaaaggaat aggcgcatta tttacacagc aagaactcca aaaacaaatg 120 ggaatcgggt cgttaacaga cttgatgtcc attgtacagg aattgctaga caagaacttg 180 atcaaattag taaaacaaaa cgacgaatta aaatttcaag gtgtcttaga atctgaggcg 240 caaaagaaag ccaccatgtc ggctgaagag gcactggtat attcttatat cgaggctagc 300 ggtagagaag ggatatggtc caagactatc aaggcaagaa ccaatctcca tcagcatgta 360 gttcttaaat gcttgaagag tttagaatcc caaagatacg tgaagagtgt taagagtgta 420 aagtttccca caaggaaaat ctacatgttg tacagcttac aaccctctgt ggacatcaca 480 ggaggtccat ggttcacaga tggagagctg gatatagaat ttatcaatag tttattgact 540 attgtttgga ggttcatatc agagaacacc ttccctaatg gcttcaagaa tttcgaaaat 600 ggacccaaaa aaaacgtctt ttatgctcca aacgtaaaaa attactctac cacacaagaa 660 attttggaat ttattacagc ggcacaagtg gccaatgtcg agttaacccc ttcaaatatc 720 agatctttgt gtgaagtctt agtgtacgac gacaagctgg aaaaagtcac gcatgactgc 780 tatagagtga ccttagagag cattctacaa atgaaccaag gtgagggcga gccggaggca 840 ggtaataagg ctttggagga tgaagaagaa ttttccatct ttaactactt caagatgttt 900 <210> SEQ ID NO 75 <211> LENGTH: 993 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 75 atgagtgaga tgttagtatc agataaagca cgtcatcttt atacaaagat gagggagtat 60 ccaacttcca aactttttga tcaagatgaa ttacaaacac tatttgatat taaaaaggga 120 tcagaattaa tggaatattt acaagaatta gtcaatggta aatatgttaa aattagtaaa 180 atgggagatc aattaaaatt tcaaactgtt gctgaagaag aagccaaaaa agtatcgtca 240 atgtctgatg atgaagcaat gatttattct tatattgaag cttcaggtcg tgaagggatt 300 tggactaaaa ccattaaagc taaaactaat ttacatcaac atattgttca aaaatgttta 360 aaaaatttag aaaataatcg atacattaaa agtattaaat cagtgaaaca tccaacaaga 420 aaaatttata tgttgtataa tttacaacct agtattgatg ttactggtgg tccttggttt 480 actgattcag aattagatac tgaatttata gaaactttat tggaagtgtg ttggagattt 540 attgttggga aaaccatgta tataaaggat gaagaagctg ataatgaaga tataaatcca 600 cttcaaacaa catatcacaa tcatcatcca ggggtgaatt tggatcaact tgttgaattt 660 ataaacaata gtaatatcac cagtgttgag ttgggtatta atgatattag atcattatgt 720 gatgtgctaa tctatgacga tagaatagaa gaagttggtg ggaatcaaga aaatagtggg 780 atttttaaag ctacttggca aagtataata gataaaggta acactatttt gcaaaataat 840 tatcaggatt tgaaaaatgt tgtttctgaa gattgtttta attatttaca acaaaatcaa 900 tcagatttta gtgtttttca atataaatct actattcaag atcttcaaga tgaatcggat 960 ctagtgtatt tagatagctg gataaatgaa taa 993 <210> SEQ ID NO 76 <211> LENGTH: 2203 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: (1657)..(1658) <223> OTHER INFORMATION: n is unknown <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: (1661)..(1661) <223> OTHER INFORMATION: n is unknown <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/U93869 <309> DATABASE ENTRY DATE: 1997-06-23 <313> RELEVANT RESIDUES: (1)..(2203) <400> SEQUENCE: 76 cgacccgggt tccgccgctt gctaccgggc tgctccgtgc atctttcccc ccaggcgtca 60 ggaactgcgc ctcatgggcg aggtgaaggt gaaggtgcag ccgcctgacg ccgatccggt 120 cgaaatagaa aacaggatta tagaattatg tcaccagttc cctcatggaa tcacagacca 180 agtaattcag aatgaaatgc ctcaatatag aagcccagca gcgggcagta gcatcaatag 240 gttgttgtct atgggtcagt tggatctctt aaggagcaat acgggccttt tatatagaat 300 aaaggactct cagaatgctg gtaaaatgaa gggatccgat aaccaagaaa aactagtata 360 tcaaatcata gaggatgcag gaaataaagg aatatggagc agagatatcc gctataaaag 420 taatttgcca ttaacagaaa tcaacaaaat tctgaagaat ctggaaagta aaaagcttat 480 caaagctgtt aagtctgtag cagcctcaaa aaagaaggtg tatatgctct ataacctgca 540 gccagaccgg tctgtgactg gtggagcctg gtacagtgac caggattttg aatctgaatt 600 tgtagaggtg cttaaccaac agtgttttaa attcctacag tccaaggcag aaacagcacg 660 agaaagcaaa cagaacccaa tgatacaaag aaatagttca tttgcctcat cacatgaagt 720 gtggaaatat atctgcgaat tgggaatcag taaggtagag ttatccatgg aagacattga 780 aaccatcctg aatacactca tttatgatgg aaaagtggag atgacgatta ttgcctgcaa 840 aagaaggcac agttggcagt gtagatggac acatgaaact gtacagggca gtcaatccaa 900 tcatccctcc cacaggtttg gtccgggcca ccctgtggac tctgccccgg tttttgatga 960 ctgccacgaa ggtggtgaga tttcaccatc taactgtatt tacatgacag agtggctcga 1020 attttaatag agagctatga actttattga cattttgcaa atgaagttac ttagggagca 1080 gataatttaa ttcatgatgg aacacgaaat ctccttgaaa gcaaacttca caataatgga 1140 cgtagacttg ctgctatgaa aacatatttt ttttatttat gaagactaaa tttatattgg 1200 taaaatagcc agtagaatat gaaagaaata aggttagtag tgaaattcat tcttcaataa 1260 ataaaacact ttgaaactcc ggaggaccac atctttcaag acttctgatg ggcgaagccc 1320 ccggcttcaa aacacgacaa ggaagtggtc tatttcgatg aatggacaat ttgaaaagat 1380 gccaacatac ccgtatttac caagtactat gataatggct agagtataaa aatgttcttt 1440 ttaaagttat ttattaagtt cttcattgga cgcttttttt tatatctggt tcactaccac 1500 cattttctgt ttcctacttt ctcagtggtt tcattgaaaa gaaattagaa ggggttaaag 1560 gcaggaatag caaagagtgc aaacttgggg tatgactggg ggagagtgga acatgccttt 1620 tccgcacaat attaattcct ttttgtatca gaaaggnnct nttaggagtt atgctaccat 1680 acttacttca aacccaatga ctactgtcaa ggtcatattt tcagtacata aatactatca 1740 ttttcattct aaagaatatt ttcactgttc cttctttctt aaagtcttat gtttcactct 1800 ttaactcaaa tgtattcttt gttagaattt accctagatt cttatttaat gtctgcagta 1860 gactgaatgt ttgtgtgccc ccagaattct aatgttgaaa tctcatttcc aatgtgatgg 1920 tatttggagg tggggctttt ggtaagtgat aggtcaggag agtaacagcg ctcatgaatg 1980 ggattagtgc ccttatataa agagacccag agagctccat caccccttct gccatgtgaa 2040 agggagaaga caaacatcca cgaaccagga agtgggtcct caccagaaaa caaatctgta 2100 agcaccttga tcttggactt cccagcctcc agaattgtga gaaataaatt tctgttgttg 2160 attttttttt tttttttttt tttttttttt tttttttttt ttt 2203 <210> SEQ ID NO 77 <211> LENGTH: 588 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/CAA96194.1 <309> DATABASE ENTRY DATE: 1997-08-11 <313> RELEVANT RESIDUES: (1)..(588) <400> SEQUENCE: 77 atgtccgggt cgttaaaatc tctagacaag aaaatagcta aaagaaggca ggtgtataag 60 cccgtgctag acaatccgtt cacaaacgaa gcacatatgt ggccgcgcgt gcatgatcag 120 ccattgattt ggcagctgct gcaatcctct atcataaata agttgattca cattcaatcg 180 aaggagaact acccttggga gctgtataca gatttcaatg aaattgtgca gtatttgagc 240 ggcgctcacg gaaacagcga cccagtatgt ctatttgtgt gcaataagga ccctgatgta 300 ccgcttgtgc tcttgcagca aatcccgcta ttatgctata tggcgcccat gacggttaaa 360 ctggtgcagt tgcccaagag tgccatggat accttcaagt cggtttctaa atatggaatg 420 ctgctgctgc ggtgcgacga tagggtcgac aagaaattcg tatcgcagat ccagaagaac 480 gttgatctgc ttcagtttcc ctggttaaat gctatcaagt atcggcccac atctgtcaag 540 ctgttgaaaa ctacagtgcc aattgtctcg aagaagaggc aaaagtag 588 <210> SEQ ID NO 78 <211> LENGTH: 663 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 78 atgaataaat caaataaagt caagaaacct tcggtggcca aagtctcaac taaagctgct 60 tcatcatcac tcaagtctca ggaagcaaag agaaaacaag ttttccgtcc aattctcgat 120 aactcattta cacaatcaaa ccaatggcca tttatagaac caactattgc aaacgatatt 180 gttgatctac tagaagtatt gctaaaaatg caagactcta catttaaata ccgtgggttt 240 aatccaactg tgtctgctct tgaaaaacaa gcagctgcta atcgtggtat acataaaaat 300 gcttgtgtac aaataaagta tgtatttgtg tgcaagtacg atatatcccc agcaacgctc 360 acaaatgtgt ttcctacgtt gtgtttcacg gcgtcaaaaa gtgctgaaga tcgggttaag 420 ctaatccagt taccaagagg aagtctagaa cggttatcga aagcacttgg ggtagataga 480 gttggtatat ttggtctaac taaagatact gaaggggcac aaccgttatt tgatcttata 540 aatgaaaatg tcaaagatat tgaagctcct tggctagact gtattttccg tgaggagatg 600 gtatttaatc aacctaacac aaagcatgtg gcaagtactg taggtagaaa gaaaaacaag 660 tag 663 <210> SEQ ID NO 79 <211> LENGTH: 960 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/CAA82141.1 <309> DATABASE ENTRY DATE: 1997-08-11 <313> RELEVANT RESIDUES: (1)..(960) <400> SEQUENCE: 79 atgagtaaaa acagggaccc tctactggct aatttgaacg ctttcaaaag caaagtgaag 60 tctgccccgg tgatcgcacc cgctaaagtt ggacagaaga agaccaatga cacagtgatt 120 actatagatg gaaacactag gaagaggacg gcctccgaac gtgcgcaaga aaacactttg 180 aactctgcga aaaatcctgt gttagtggat atcaagaaag aagctgggag caatagctct 240 aatgctattt cattagatga cgacgatgac gacgaagatt ttggtagctc tccttcaaaa 300 aaagtaaggc ctggctctat tgctgcagcc gctttacaag caaatcaaac agatatttcc 360 aagagtcacg attcttcaaa gttgctttgg gcgactgaat acattcaaaa gaaaggtaag 420 cccgttttgg tgaatgagtt attggactac ttgtcaatga aaaaagatga caaggttatt 480 gagcttttaa aaaaattaga tagaatagag tttgacccca agaaggggac tttcaaatac 540 ctttccacct acgatgtcca ttccccttcg gaactgctga agttgttacg ttcacaagta 600 acattcaaag gtatttcctg caaagacttg aaagacggtt ggccacaatg cgatgaaacg 660 attaaccaac tggaggaaga cagcaaaatt ttggtgttaa gaactaaaaa ggataaaact 720 ccaagatacg tttggtataa cagcggtggt aacttgaaat gtattgacga ggagtttgtt 780 aaaatgtggg aaaatgtgca attaccgcaa tttgcagaat tgccaagaaa gctgcaagat 840 ttaggtctaa agcctgctag tgtcgatcct gctactatca aaagacaaac aaagagagtt 900 gaagttaaaa agaagagaca aagaaagggt aagattacta acactcatat gaccggtatc 960 <210> SEQ ID NO 80 <211> LENGTH: 855 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 80 atgtccgact tatcagctca actttcagct tttaagaata agatcaaaag tggaccatcg 60 gtgattgttc ctagaaaggc aacttttact caatctccat catcaccatt atcatcatca 120 accacaacaa caacactgaa gaatgacgcc aatgtgaaga agagatcaac gacggattca 180 gtaacccgag tattgaagaa acaaaaggca aatatgggag aaatgacggg atcacattta 240 tcgacacaat tacaccttgc tgttgaatat atcaaggaac atgaccaacc aatatcggtg 300 gagaagttgc agaattattt atcatttgat atatcacata ctttattgcc attattgaat 360 gaaattgatc gagtgaaata cgacgaatct aagggtacat tggaatatgt ttcattgcat 420 aatattcgta gtagtgatga tttattggaa tttttgagac gtcaaaccac attcaagggc 480 acttccgtaa aagaattaaa agatggttgg gctggttgtg ttgccgctat agacgaatta 540 gaatcacaag gcaaaatttt ggtgttgcgt aacaagaagg aaaatgctcc aagattagta 600 tgggctaata atggtggtga gttgggttat attgacacag aattcaagga tatgtgggat 660 caagtgaaat tgccggaacc agatgtattg tatcagaaat tattggatca aggattgaaa 720 cctacgggag ctgatcctaa tttgatcaaa aagcaaccac aacaaaagga aaagaaacaa 780 aagaaagcaa gaagaggaaa gattacaaat acacatatga aaggtatttt gaaggattat 840 tctcaattag tttga 855 <210> SEQ ID NO 81 <211> LENGTH: 1500 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/NM_002095.1 <309> DATABASE ENTRY DATE: 2000-10-30 <313> RELEVANT RESIDUES: (1)..(1500) <400> SEQUENCE: 81 cttaaattac ccactacgtt gtccagtcgc cgcctcagct accgccgctg ccgccgccgc 60 cgccgccacc gccagtggtg agaccccgac ctggcgggtc agcgctgggc gtgcgtgcgg 120 gcaggcgggg gcgctgacga gaagcaggaa gagggtgcag tgccggcgtg ggcggccggc 180 cgaggcggag gcgcaggaag ggggcggcga gtcgtgcgag gctgcccttc tcactcagca 240 ttatggatcc aagcctgttg agagaaaggg agctgttcaa aaaacgagct ctttctactc 300 ctgtagtaga aaaacgttca gcatcttctg agtcatcatc atcatcgtca aagaagaaga 360 aaacaaaggt agaacatgga ggatcgtcag gctctaaaca aaattctgat catagcaatg 420 gatcatttaa cttgaaagct ttgtcaggaa gctctggata taagtttggt gttcttgcta 480 agattgtgaa ttacatgaag acacggcatc agcgaggaga tacgcatcct ctaaccttag 540 atgaaatttt ggatgaaaca caacatttag atattggact caagcagaaa caatggctaa 600 tgactgaggc tttagtcaac aatcccaaaa ttgaagtaat agatgggaag tatgctttca 660 agcccaagta caacgtgaga gataagaagg ccctacttag gctcttagat cagcatgacc 720 agcgaggatt aggaggaatt cttttagaag acatagaaga agcactgccc aattcccaga 780 aagctgtcaa ggctttgggg gaccagatac tatttgtaaa tcgtcccgat aagaagaaaa 840 tacttttctt caatgataag agctgtcagt tttctgtgga tgaagaattt cagaaactgt 900 ggaggagtgt cactgtagat tccatggacg aggagaaaat tgaagaatat ctgaagcgac 960 agggtatttc ttccatgcag gaatctggac caaagaaagt ggcccctatt cagagaagga 1020 aaaagcctgc ttcacagaaa aagcgacgct ttaagactca taacgaacac ttggctggag 1080 tgctgaagga ttactctgac attacttcca gcaaataggg aacagttttg ccctggaaca 1140 gagttacaga tacacaatca agagtgttct tgctgatgct cggggtctga agactgtctt 1200 cctatctgct tcttgcggct gaggagagga gcagttcagt ttacaaaaca agtgcaaatt 1260 accaaactca aagcttattt gagtagaatg ggctcatggg caatgtgatg ttccctgtta 1320 accttctgtt actccctggg agaaaggcgc tgagcgtggc atgcaggtgt ctttgctgtg 1380 tttttctcca cttctaaatg gttcctggtt cctttcttcc tcgtttgtta ctttagagca 1440 agtttgccca tagtcttgaa tgcaatattt gtttattcca aaagaacata tttataataa 1500 <210> SEQ ID NO 82 <211> LENGTH: 1560 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/CAA96830.1 <309> DATABASE ENTRY DATE: 1997-08-11 <313> RELEVANT RESIDUES: (1)..(1560) <400> SEQUENCE: 82 atgtctcaag aacagtacac agaaaacttg aaggttatcg ttgccgaaaa actggctggt 60 ataccaaact ttaacgaaga tatcaagtat gttgcggagt atattgtctt attgatcgtt 120 aacggtggta ctgttgaatc tgtcgtagac gagctggcta gtttgtttga tagtgtttcg 180 agagatacgc ttgcaaatgt tgttcaaaca gcctttttcg cattagaagc tctgcaacag 240 ggagaaagtg ctgaaaatat tgtttccaaa attagaatga tgaatgcgca aagcttggga 300 caatcggata tcgcacaaca gcaacaacag caacaacaac aacagcaacc agacatcgcg 360 caacagcaac ctcaacagca acctcaacag caacctcaac agcaacctca acagcaacct 420 caacagcaac ctcaacagca acctcaacag caacctcaac agcaacctca acttcaacca 480 cttcagccac aactagggac ccagaatgca atgcagacag atgctcctgc aactccatcc 540 cccatatcag ccttttccgg cgttgttaac gctgcagctc cccctcagtt tgcgcctgta 600 gataacagcc aaaggttcac tcaacgtggc ggaggcgccg ttggaaagaa tcgtagaggt 660 ggtcgcggtg ggaaccgtgg aggacgcaac aataattcca cacgttttaa tccgttagca 720 aaagcacttg gaatggcggg tgagagtaat atgaacttca ctccaaccaa gaaagagggg 780 cgttgcagat tgtttcctca ctgtcctctt ggtagatcat gcccacatgc acacccaact 840 aaggtatgta atgaatatcc aaattgtcca aagcctcccg gaacttgtga gtttttacat 900 ccaaatgaag atgaagagtt gatgaaggaa atggaaagaa ctcgtgaaga atttcaaaaa 960 agaaaagctg atttattggc ggcaaaaagg aaaccggtac aaactggtat cgttctgtgt 1020 aaatttgggg ctctgtgttc caatccatca tgcccatttg gtcatccaac accagcaaat 1080 gaagatgcga aagtcattga tctaatgtgg tgtgacaaga atttgacatg tgataatcct 1140 gagtgtagaa aggcccactc ttcattgtcg aagatcaagg aagtaaaacc aataagccag 1200 aagaaagcag ctccacctcc ggttgaaaag tccttagaac aatgtaagtt cggtacgcac 1260 tgcaccaata aacgttgcaa atatagacat gctcgttctc atattatgtg ccgtgaagga 1320 gcaaactgta ctagaattga ttgtttattt ggccatccaa ttaatgaaga ttgtagattt 1380 ggtgtcaatt gtaagaatat ttactgtcta ttcagacatc ctccaggcag agtacttccg 1440 gaaaagaaag gcgctgcacc caattcaaac gttcctacca atgaaaggcc atttgcattg 1500 ccagaaaacg caataattga aaatgctcct ccgcaaacca gttttacgca ccaagaacaa 1560 <210> SEQ ID NO 83 <211> LENGTH: 1296 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 83 atgcaatttg ctccagataa ccaaataggc aaagagttac agcaaaactt gattcaagaa 60 atacaaaggc gtttcaataa accggctgat gatgccgtag atattgctga ctatatcatc 120 tacttgattg tggcaaaaaa gagcgaacaa gaaatagtcg cagaagtcaa agatattgct 180 gacatatcta ttgatgttgg gtttattggg gatgtttatc tggaaatcag aaagttggaa 240 gtaaaatata atcaacctcc tgctgcagtg gaggaagctt ctcaacctca acaagaacag 300 caacagcaat ctcaagcttc tgtagtggct ccacaaattc ctattggtcc taagaaacaa 360 ttaactgagg aagagaagat tgcccttcga agtcaaagat ttggaactac tactagattg 420 agtgggcgag gtggacgtgg tggtataact aaaactagaa ccgatttcag aaatgggcac 480 aataataaga acttcctaga ccctaaaaaa ttagaccaaa taatttctgg tgccaataat 540 ggggctatta agtttgtacc actcccacca aaaggtagat gtccagattt cccatattgt 600 aagaatcaga attgtgaaaa agctcatcca acaaaaaact gtttcaacta cccggattgc 660 cctaacccac cgggaacatg taattttttg catccggatc aagaccaaga gttgattgct 720 aaattagaaa catctaaaaa agaatttgaa gaaaagaaaa agaatcaact tatggtcaaa 780 caaggctcat gtaaatatgg tttgaaatgt gctaaagaaa attgtccatt tgctcaccca 840 acaccagcta atcctgaatc tggtaagatt gaaactttgg aatggtgtcc acaaggtaag 900 aattgtcaag atagaaattg tactaaatca catccacctc cacctacggc aaactcagaa 960 aaattattat cagctgctga cttggcattg gaacaatgta aatttggttc acaatgtact 1020 aatctcaaat gtccaagaag acatgcaact tcggctgtgc catgtcgtgc tggtgctgaa 1080 tgtagaagag tcgattgtac attttcccat ccattgaaag aaccatgccg ttttggaaca 1140 aaatgtacaa ataaagtgtg tatgtaccaa catcctgaag gaagaactat tgcctctcac 1200 acttggacca aggatggtag tggcaataat aacagtacct caaatcgatc atttgctgtt 1260 tctgaagatc agattatgga acaagttgct caatag 1296 <210> SEQ ID NO 84 <211> LENGTH: 680 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/AF155107.1 <309> DATABASE ENTRY DATE: 2000-01-05 <313> RELEVANT RESIDUES: (1)..(680) <400> SEQUENCE: 84 acccacagca gttgcacttg ctgagcaggc agcttgagga cccaaatggt agcttttcta 60 acgctgagat gagtgaactg agtgtggcac agaaaccaga aaaacttttg gagcgctgca 120 agtactggcc tgcttgtaaa aatggggatg agtgtgccta ccatcacccc atctcaccct 180 gcaaagcctt ccccaattgt aaatttgctg aaaaatgttt gtttgttcac ccaaattgta 240 gatacggaaa tgaactgaaa tatgatgcaa agtgtactaa accagattgt cccttcactc 300 atgtgagtag aagaattcca gtactgtctc caaaaccagt tgcaccacca gcaccacctt 360 ccagtagtca gctctgccgt tacttccctg cttgtaagaa gatggaatgt cccttctatc 420 atccaaaaca ttgtaggttt aacactcaat gtacaagacc ggactgcaca ttctaccatc 480 ccaccattaa tgtcccacca cgacatgcct tgaaatggat tcgacctcaa accagcgaat 540 agcacccagt cctgcctggc agaagatcat gcagtttgga agttttcatg tctgatgaaa 600 gatctctaca gaacttgtca aatctttgaa acttggaata tattgctttc ataatatgaa 660 ggtttattgg ctatctaaaa 680 <210> SEQ ID NO 85 <211> LENGTH: 1140 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/CAA88520.1 <309> DATABASE ENTRY DATE: 1999-02-10 <313> RELEVANT RESIDUES: (1)..(1140) <400> SEQUENCE: 85 atggcaaatt cgccgaaaaa gccatctgat ggcactggag tatcagcgtc agacacgcct 60 aaatatcaac ataccgtccc agaaacgaaa ccagcattta atttgtcacc aggtaaagct 120 agtgagctat cacatagcct tccgtcgcct agccagataa aatcaaccgc acatgtatct 180 tcaactcaca atgatgcggc aggtaatacg gatgattctg ttcttcctaa aaatgtatca 240 cccacaacta atttgagagt tgaaagtaat ggagatacaa acaatatgtt ctctagccct 300 gctggactag ctctaccaaa aaaggatgat aaaaaaaaaa acaagggtac gagtaaagca 360 gattctaaag atggcaaagc atccaactcc tcaggacaga atgcacaaca acaatcagac 420 ccaaataaaa tgcaagatgt ccttttttcc gcaggtatcg atgttaggga ggaggaggct 480 cttctaaatt catctattaa tgcctcaaaa tcccaagttc aaacaaataa cgttaagatc 540 cccaaccatt taccattcct tcacccggaa caagtttcca attatatgag gaaagtcgga 600 aaagagcaaa acttcaacct gacccctaca aagaatcctg aaattttgga catgatgtca 660 agtgcctgcg aaaactatat gagagatatc ctaacaaatg ccattgtcat ctcccgacat 720 agaagaaaag cagtcaagat aaattctggt agaagaagtg aagtttctgc ggctttaaga 780 gccattgcac taattcaaaa aaaagaagaa gaaaggcgtg tgaaaaaaag aattgcgttg 840 ggactcgaga aggaagatta tgaaaataag attgattccg aagagacgtt acacagagca 900 tcgaacgtta cggctggcct tagagcaggt agtaaaaaac agtatggttg gctaacttca 960 tcagtaaata agccgacgtc cttgggagca aaatcttcag gcaaagtcgc ctccgacatc 1020 acggctagag gagaaagtgg gctaaagttt agagaagcta gagaggagcc tggtatagta 1080 atgagggatt tactctttgc tctcgaaaat aggcgcaaca gcgttcagac tattatttca 1140 <210> SEQ ID NO 86 <211> LENGTH: 1119 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 86 aatcaccgaa ttatatcaca taaatccatg acaagtacac ctcaagaatc ctctaattta 60 aagagacaat tagaaaacag tgaggactcc agctcaccaa ataaggaatc taaaacagag 120 actaccacgg aaaaccagag ctcatgggag tctgacttta atagtttacc agtggaatta 180 ctacaaactg aaacaaatgg tacatcacca gcaccagcac cagcaacacc gatcgatacc 240 accaatgcat caagcacaaa ggaacgtgat caggatactt ctaaattaaa tgacgcgatt 300 gctgctgcag gagttgatat tcaacaagaa gaagagatat tattacaaca acaattaaat 360 agaaaatctg cagagggtat ggcaagcaat ctaaaaagtg tgatcaggtc cagcaaactg 420 cctccatttc tacacaatta ccatttagct gcctttattg ataaagtggc taaacaaaat 480 ggaattcaac agaatttctt aatggatggt gagatgttgg aattaatttc agctgcttgt 540 gagacttggt taagtaatct agcaacaaaa acgataatct tgtcacgcca caggagaagg 600 ggaatacctg ttattaataa gaagtcagga agtagttcag ttccaagatc agaaatttca 660 aaagaattga gaagcttggc cttaaaacaa aaggaaatgg aagagaaacg agtgaataaa 720 agagtgatgt tggggttgga aaaaagcacc aaagacgcat ccaaaaatga cgaaaatggt 780 gaatcaaaag ctggtgctga agaaacatta catcgtgcag caaatgctac agctgcaatg 840 atgactatga atcccgggag aaagaaatat agttggatga cttcaagtgc tacagcaggc 900 ggtgggtcag actttggtaa atcaagtggt ggctcatcaa aggactcggg aaaacaccaa 960 agtcctatta tttcagtacg tggtgataat ggccttaggt ttagagaaat aaggtcaggt 1020 aattccatta ttatgaaaga tttgttaggc gcaattgaag atgaaaaaat gggtacgaga 1080 aatgctgtaa taaaaggata tgcaaaattg aaagattaa 1119 <210> SEQ ID NO 87 <211> LENGTH: 2307 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/Y11354.1 <309> DATABASE ENTRY DATE: 1997-06-25 <313> RELEVANT RESIDUES: (1)..(2307) <400> SEQUENCE: 87 atggcggcgg gctcggatct gctggacgag gtcttcttca acagcgaggt ggacgagaaa 60 gtggtgagcg acctggtggg ctcgctggag tcgcagctgg cggccagcgc ggcccaccac 120 caccacctcg cgccgcgcac gcccgaggtg cgggccgcgg ccgccggcgc gctcgggaac 180 catgttgtga gcggcagccc ggccggagcc gcgggcgcag ggccggccgc ccccgccgag 240 ggcgcgcccg gagcggcgcc ggagccgccc cccgcaggta gagcgcggcc ggggggcggg 300 gggccgcagc gcccgggccc cccctcaccg cgccgccccc ttgtccccgc agggcccgcg 360 ccgcccgccg cgaagctgag gccgccgccc gagggcagcg cgggggcctg cgccccggtg 420 cccgccgccg ccgccgtcgc cgcggggccc gagcccgccc ccgccggccc cgccaagccc 480 gccggccccg ccgcgctggc cgcccgcgcc ggccccggcc ccgggcccgg ccccggcccc 540 ggccccggcc ctggcaagcc cgccggcccc ggcgccgcgc aaactttgaa tgggagcgcc 600 gcgctgctga actcgcacca cgccgccgca cctgctgtca gcctggtcaa caacgggccc 660 gccgcgctgc tgccgctgcc caagcccgcc gcccccggca ctgtcatcca gacgcccccc 720 ttcgtgggcg ccgccgcgcc ccccgcgccc gccgcgccct cgccccccgc cgcccccgcg 780 cccgccgccc ccgccgccgc cccgcccccg ccaccccccg cgcccgccac cctggcccgg 840 ccgcccggcc accccgccgg acccccgacc gccgcgcccg ccgtgccgcc ccccgccgcc 900 aagggttatg ccaagatcag agattaagcc cagaacgggg gcagcgccgg ggcagccccc 960 gcccccgccc cggccgccgg gggccccgct ggggtcagcg gccagcccgg gcccggcgcg 1020 gcggctgcgg cgccggcgcc gggggtcaag gccgagtcgc ccaagagggt ggtgcaggcg 1080 gcgcccccgg cggcgcagac cctggcggcc agcggcccgg ccagcacggc ggccagcatg 1140 gtcatcgggc caactatgca aggggcgctg cccagcccgg ccgccgtccc gccgcccgcc 1200 cccgggaccc ccaccgggct gcccaaaggc gcggccggcg cagtgaccca gagcctgtcc 1260 cggacgccca cggccaccac cagcgggatt cgggccaccc tgacgcccac cgtgctggcc 1320 ccccgcttgc cgcagccgcc tcagaacccg accaacatcc agaacttcca gctgccccca 1380 ggaatggtcc tcgtccgaag tgagaatggg cagttgttaa tgattcctca gcaggccttg 1440 gcccagatgc aggcgcaggc ccatgcccag cctcagacca ccatggcgcc tcgccctgcc 1500 acccccacaa gtgcccctcc cgtccagatc tccaccgtac aggcacctgg aacacctatc 1560 attgcacggc aggtgacccc aactaccata attaagcaag tgtctcaggc ccagacaacg 1620 gtgcagccca gtgcaaccct gcagcgctcg cccggcgtcc agcctcagct cgttctgggt 1680 ggcgctgccc agacggcttc acttgggacg gcgacggctg ttcagacggg gactcctcag 1740 cgcacggtac caggggcgac caccacttcc tcagctgcca cggaaactat ggaaaacgtg 1800 aagaaatgta aaaatttcct atctacgtta ataaaactgg cttcatctgg caagcagtct 1860 acagagacag cagctaatgt gaaagagctc gtgcagaatt tactggatgg aaaaatagaa 1920 gcagaagatt tcacaagcag gttataccga gaacttaatt cttcacctca accttacctt 1980 gtgcctttcc tgaagaggag cttacccgcc ttgagacagc tgacccccga ctccgcggcc 2040 ttcatccagc agagccagca gcagccgcca ccgcccacct cgcaggccac cactgcgctc 2100 acggccgtgg tgctgagtag ctcggtccag cgcacggccg ggaagacggc ggccaccgtg 2160 accagtgccc tccagccccc tgtgctcagc ctcacgcagc ccacgcaggt cggcgtcggc 2220 aagcaggggc aacccacacc gctggtcatc cagcagcctc cgaagccagg agccctgatc 2280 cggcccccgc aggtgacgtt gacgcag 2307 <210> SEQ ID NO 88 <211> LENGTH: 555 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/CAA82029.1 <309> DATABASE ENTRY DATE: 1997-08-11 <313> RELEVANT RESIDUES: (1)..(555) <400> SEQUENCE: 88 atgaacacca atagtaatac tatggtaatg aatgacgcaa atcaagcaca aataacggcc 60 acatttacga agaagatatt agcgcatttg gatgatccgg actccaacaa attggcccaa 120 ttcgtacagc tttttaatcc aaacaactgc agaataatat ttaatgctac ccccttcgcg 180 caagcaacag tttttctgca aatgtggcaa aaccaggtcg tacaaacaca acatgcccta 240 acaggagtag actatcacgc tattccggga tccggcacgt tgatatgcaa cgtcaattgc 300 aaagtcagat tcgacgaaag cggcagagac aagatggggc aagacgcgac tgttcccatt 360 caaccaaata acactgggaa cagaaatcga cccaacgata tgaacaagcc aagacctcta 420 tggggtccat attttggcat ttccctgcag ctgatcatcg acgaccgcat atttagaaat 480 gattttaatg gtgtaatatc ggggtttaac tataacatgg tttacaaacc cgaggattct 540 ctgctaaaaa tttag 555 <210> SEQ ID NO 89 <211> LENGTH: 540 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 89 catcctatag cacaacaact agagccgttt ctcaaacgat ttcttgcatc gttagattta 60 ctgtacacac agccaacatc acaaccattc cccaacgttg aatcgtatgc cactcagtta 120 ggatcaaact taaagcggtc aagtgcaatt atagtgaacg gccagcctat tataccgagc 180 ccacaagaag actgtaaatt acaattccaa aagaaatggt tacaaactcc gttatcgtca 240 caccaattga caagttacga tgggcattta attccaggca cggggacctt tgtcgttcat 300 ttttcagcaa aagtaagatt tgatcaaagt ggaaggaacc ggttaggtga atctgccgac 360 ttgtttcagg aaaataattc aattgtttcc aaaaccaatc aaagacctat ttggggttcg 420 tggtttggag tcgacgtcaa tttggttgtt gacgaaaacg ttatgcaaga tggagagatt 480 ataaatagta tggattatag atttacctat gtacctaacg atagcattat aaaagtataa 540 <210> SEQ ID NO 90 <211> LENGTH: 720 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/CAA97636.1 <309> DATABASE ENTRY DATE: 1997-06-17 <313> RELEVANT RESIDUES: (1)..(720) <400> SEQUENCE: 90 atgaacgctc tttacaacca tgctgtgaag caaaaaaatc aactacaaca agagttggcc 60 aggtttgaaa agaattctgt gaccgcccct atttctttac aagggtccat ctctgcaact 120 ctggtctcac tggagaaaac agttaagcaa tatgcagaac atttaaacag atataaagaa 180 gatactaatg cagaggaaat tgatcctaag ttcgctaatc gactagcaac tttaacacag 240 gatctgcacg actttactgc caagtttaag gatttaaaac aatcctacaa cgaaaataat 300 tccagaactc agttgtttgg ctcaggagca tcgcatgtta tggactccga taaccccttt 360 agtacatcag agaccatcat gaataaaagg aacgttggtg gtgcgagtgc aaatggtaaa 420 gagggctcta gcaacggtgg gggactaccg ttgtaccaag ggctacaaaa ggaacagtct 480 gttttcgaaa ggggtaacgc tcaattagat tacattctag aaatgggcca acaatcattc 540 gaaaatatag tggaacaaaa caaaatttta tccaaggtac aagatagaat gtcaaatggc 600 ctaagaacat tgggtgtttc ggaacaaact atcacctcta tcaataaacg ggtgttcaaa 660 gataaactag tcttttggat cgcgttaatt ctcttgatca taggtattta ttatgtgttg 720 <210> SEQ ID NO 91 <211> LENGTH: 483 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 91 atgaattcaa tatataatca tggtttaaaa caaacccaaa ctataactaa agatttaact 60 caattcgaga aaaacttatc cacatcacca ttatcattac aagtgcaatc acaacatcat 120 taactgcatt caggaaaact atcgaagaat atgatgattt attggaagta aatgtctatg 180 atacatctga taccatagat gagggtagat tagatatatt caatccagat ttaaatgaat 240 acactctgaa atatgatact ttaaataagc tacgtgagtt tcttctccat caagctaata 300 aacaagaatt attaggagaa ggacacttat caccaacagc aacagcagca ttggatcgac 360 atcatcagat aatccgtatg aatctagctc aaatccatct caacaacaac aacagcaatt 420 acaagatgaa caaaacacca tgtcttatag agaaggatta tatcatgaaa agaattctct 480 aga 483 <210> SEQ ID NO 92 <211> LENGTH: 1560 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/NM_003569.1 <309> DATABASE ENTRY DATE: 2000-11-01 <313> RELEVANT RESIDUES: (1)..(1560) <400> SEQUENCE: 92 gagggagccg tggaggtcca ggtgactgct tagaaaactg cacagcatct gatgaaatta 60 gcgaataaga acatcaacca tgtcttacac tccaggagtt ggtggtgacc ccacccagtt 120 ggcccagagg atctcttcta acatccagaa gatcacacag tgttctgtgg aaatacaaag 180 aactctgaat caacttggaa cacctcaaga ttcacctgaa ttgaggcaac agttgcaaca 240 gaagcagcag tatactaacc agcttgccaa agaaacagat aagtacatta aagagtttgg 300 atctctgccc accaccccca gtgaacagcg tcaaaggaaa atacagaagg atcgcttagt 360 ggcagagttc acaacatcac tgacaaactt ccagaaggtc cagaggcagg ctgctgagcg 420 agagaaagag tttgttgctc gagtaagagc cagttccaga gtgtctggca gttttcctga 480 ggacagctca aaagaaagga atcttgtatc ctgggaaagc caaactcaac ctcaagtgca 540 ggtgcaggat gaagaaatta cagaggatga cctccgtctt attcatgaga gagaatcttc 600 tatcaggcaa cttgaagctg atattatgga tattaatgaa atatttaaag atttgggaat 660 gatgattcat gaacaaggag atgtaataga tagcatagaa gccaatgtgg aaaatgcaga 720 ggtgcacgtt cagcaagcaa atcagcagct gtcaagggca gcagattatc agcgcaaatc 780 cagaaaaacc ctgtgcatca tcattcttat ccttgtcatt ggagttgcga ttatcagtct 840 catcatatgg ggattgaacc actgaagtta taaaggagca cactgtcgca ctacattgtc 900 taaattatgt aggaagattc ctgtaatcat gtttttttaa ttattatttt aaagctattg 960 tataaaggat ggttcccata ctttgttatt tttattgggg gggttgggcg ggttcctttg 1020 gattaaatct gatattttct aatactgaaa gattttctaa atgtcactgc tgacataact 1080 cccttggtct tcaatttaat agttgttaag ttttgggcca cattgcatat gcctttcatt 1140 tataatttat ttaccctgct tgacttagtt tggggaattc ggaaatttaa ggtgtgtgta 1200 ttctgttggg atctccctgc cacgtgaaca caccaagatg tgtgttactt caagttaaaa 1260 ctccccaaaa tttaattttt gatttgcttc caccagggga aaatattctc caataatgta 1320 aaataattaa ggtccaatac atgggttgta tttttctggt tcacaacagc acaaagtgtc 1380 tttcattttt ttgttggatt tcctttaaga tcttttttac cctgaagtcg gtgaacactt 1440 ttctagttaa tttgatactc tttctgtgta tataataagc ttttgctgta gattgcctag 1500 taaaattact aaggataggt tgtttttaca tatggtctat ttaagtctga tgtttacggg 1560 <210> SEQ ID NO 93 <211> LENGTH: 720 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/CAA85038.1 <309> DATABASE ENTRY DATE: 1999-06-24 <313> RELEVANT RESIDUES: (1)..(720) <400> SEQUENCE: 93 atgttagaag caaaatttga agaagcatcc cttttcaaga gaataattga tggtttcaaa 60 gattgtgtcc agttggtcaa tttccaatgt aaagaagatg gtatcattgc acaagctgtc 120 gatgactcaa gagttctatt ggtctccttg gaaataggtg tcgaagcctt ccaagaatat 180 agatgtgacc atcctgttac gttaggtatg gatctaacct cactaagtaa aatcctacgt 240 tgtggtaaca acaccgatac attaacacta attgctgaca acacaccgga ttccatcatc 300 ttattatttg aggataccaa gaaagaccgt atagccgaat actctctgaa attgatggat 360 atcgatgctg atttcttaaa gattgaagaa ttacagtacg actccaccct gtcattgcca 420 tcttccgaat tctctaaaat tgttcgtgac ttgtcccaat tgagtgattc tattaatatc 480 atgatcacca aagaaacaat aaagtttgta gctgacggtg atatcggatc aggttcagtc 540 ataataaaac cattcgtgga tatggaacat cctgaaacaa gcatcaaact tgaaatggat 600 caacctgtcg acttgacgtt cggagctaaa tatttattgg acatcattaa gggctcctcc 660 ctttctgata gagttggtat caggctctcc agcgaagctc ctgctttatt ccaatttgat 720 <210> SEQ ID NO 94 <211> LENGTH: 780 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 94 atgttagaag gtaaatttga agaagctgct ttattaaaaa aagttgttga agccattaaa 60 gattgtgtta aaaaatgtaa cttcaattgt tcagagcatg ggattactgt acaagcagtg 120 gatgattctc gtgtattatt agtttcatta ttaattggtc aaacttcttt cagtgaatat 180 agatgtgaca gagacgttac attaggtatt gacttggaaa gtttcagtaa gattatcaaa 240 tctgctaaca atgaagattt cttgaccctt ttagctgaag attcaccaga tcaaataatg 300 gctattcttg aagaaaaaca aaaagagaaa atcagtgaat attctttaaa attaatggat 360 attgattctg aatttttaca aattgatgat atggaatacg atgctgttgt gaatatgcca 420 agtagtgatt ttgctaaact tgtgagggat ttgaaaaatt taagtgaatc tttacgtgtt 480 gttgttacta aagattccgt caagtttaca tctgaaggtg attctggttc cggaagtgtt 540 atcttgaaac cttacaccaa cttgaaaaat gaaagagaaa gtgtcactat tagtttagat 600 gacccagttg atttgacttt tggtttgaaa tacttgaatg atattgtgaa ggcagctaca 660 ttatccgatg tcatcaccat caaattggcc gataaaactc ctgcattgtt tgaatttaaa 720 atgcaatctg gaggttattt gagattctac ttggcaccaa aattcgatga tgatgagtag 780 <210> SEQ ID NO 95 <211> LENGTH: 1200 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/GI:181271 <309> DATABASE ENTRY DATE: 1993-04-27 <313> RELEVANT RESIDUES: (1)..(1200) <400> SEQUENCE: 95 aggtctcagc cggtcgtcgc gacgttcgcc cgctcgctct gaggctcctg aagccgaaac 60 tagctagact ttcctccttc ccgcctgcct gtagcggcgt tgttgccact ccgccaccat 120 gttcgaggcg cgcctggtcc agggctccat cctcaagaag gtgttggagg cactcaagga 180 cctcatcaac gaggcctgct gggatattag ctccagcggt gtaaacctgc agagcatgga 240 ctcgtcccac gtctctttgg tgcagctcac cctgcggtct gagggcttcg acacctaccg 300 ctgcgaccgc aacctggcca tgggcgtgaa cctcaccagt atgtccaaaa tactaaaatg 360 cgccggcaat gaagatatca ttacactaag ggccgaagat aacgcggata ccttggcgct 420 agtatttgaa gcaccaaacc aggagaaagt ttcagactat gaaatgaagt tgatggattt 480 agatgttgaa caacttggaa ttccagaaca ggagtacagc tgtgtagtaa agatgccttc 540 tggtgaattt gcacgtatat gccgagatct cagccatatt ggagatgctg ttgtaatttc 600 ctgtgcaaaa gacggagtga aattttctgc aagtggagaa cttggaaatg gaaacattaa 660 attgtcacag acaagtaatg tcgataaaga ggaggaagct gttaccatag agatgaatga 720 accagttcaa ctaacttttg cactgaggta cctgaacttc tttacaaaag ccactccact 780 ctcttcaacg gtgacactca gtatgtctgc agatgtaccc cttgttgtag agtataaaat 840 tgcggatatg ggacacttaa aatactactt ggctcccaag atcgaggatg aagaaggatc 900 ttaggcattc ttaaaattca agaaaataaa actaagctct ttgagaactg cttctaagat 960 gccagcatat actgaagtct tttctgtcac caaatttgta cctctaagta catatgtaga 1020 tattgttttc tgtaaataac ctattttttt tctctattct ctccaatttg tttaaagaat 1080 aaagtccaaa gtctgatctg gtctagttaa cctagaagta tttttgtctc ttagaaatac 1140 ttgtgatttt tataatacaa aagggtcttg actctaaatg cagttttaag aagtgttttt 1200 <210> SEQ ID NO 96 <211> LENGTH: 1500 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/CAA88556.1 <309> DATABASE ENTRY DATE: 1997-08-11 <313> RELEVANT RESIDUES: (1)..(1500) <400> SEQUENCE: 96 atgtcgaaaa ggtctatcga ggtcaacgag gaacaagata gagtggtctc tgctaaaaca 60 gaatctcact ctgttcctgc tattcccgcc tctgaagagc aagatgctcc caagaatgac 120 ctagaagaac aattgagtga tgaatttgat agtgatggtg aaattattga aattgatggc 180 gatgatgaga ttaatgacga agatgacctt aggaaaaagc aagaagaagc tgaaacttta 240 gtacaaaagg accaatccga aggcaacaaa gaaaagatcc aggagcttta cttaccccat 300 atgtctcgtc cattagggcc agatgaagtc cttgaggctg atcccactgt ttatgaaatg 360 ctacataatg tcaatatgcc atggccatgc ttgacattag atgtcattcc agatacacta 420 ggttctgaac gtagaaacta tccacagtct attttgttga ccacggctac tcaatcttcc 480 aggaaaaagg agaatgaact aatggttcta gcactttcta atttagcgaa aacacttttg 540 aaagacgata atgaaggtga agatgatgaa gaggatgatg aagatgatgt ggatccagtc 600 attgagaatg aaaatatacc attgagagat acaaccaata gattaaaggt ttctcctttt 660 gccatttcta atcaagaggt gttaaccgct acaatgagcg aaaatggtga tgtttatata 720 tacaatctag ctccacaaag caaagctttt tccacaccag gttatcagat tccgaagtct 780 gctaagcgtc ctattcacac tgtaaaaaat catgggaatg ttgaaggcta cgggttggat 840 tggtcaccat tgatcaagac tggtgcgtta ctatcaggtg attgctcagg acaaatatat 900 tttacccaaa ggcacacatc gagatgggtg actgataaac aaccatttac tgtttcaaac 960 aataaatcca tagaagatat ccagtggtct cgcactgaat ccaccgtttt tgcaaccgca 1020 ggatgtgatg gatatataag gatttgggac acaagatcaa aaaaacataa acctgctatc 1080 tctgttaaag cttctaatac tgacgtaaat gtcataagtt ggagtgataa aattggttac 1140 ttgctagcaa gcggtgacga taacggtaca tggggagtat gggatttaag acagtttacg 1200 ccaagtaatg ctgacgccgt ccaaccggtt gctcaatatg acttccataa gggagccatt 1260 acttccattg cattcaaccc attagatgag tctatcgttg cggtaggctc agaagataat 1320 actgtgactt tgtgggattt gtctgtagaa gctgacgatg aggaaattaa acaacaggcc 1380 gccgaaacaa aagagctaca agaaattcca ccacaattat tgtttgttca ctggcaaaag 1440 gaagttaaag atgtcaaatg gcataagcaa atcccaggtt gtttagtaag taccggtact 1500 <210> SEQ ID NO 97 <211> LENGTH: 1554 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 97 atgtcaaaaa gatcagctga agatgattta agtggcaata gatccaccag tcatactgcc 60 attaaaacta ataaagattc tcttccaact actacaaatg gaaaggaaga agaaccagac 120 aatatggata ttggggaatt tgaagatcca tacggtgatg aatttgaaag tgatgaagaa 180 attatagaat tagacgataa caatgatgaa gaagatgatg aaatgattga tgaaaattca 240 acacaagcca aaattgaaga attagaagcc aaagaacaag aacaagaaca acaatcatca 300 atatatttac ctcataaatc aaaaccatta ggaccagatg aagtcttaga agccgatcca 360 acagtctatg aaatgttgca taatatcaat ttaccatggc catgtttgac tgttgatatt 420 ttaccagatt ctttaggtaa tgaaagaaga tcatatccag caacagttta tttagctact 480 gcgactcaag ctgctaaagc caaagataat gaattgttag ctatgaaagc atcttcattg 540 gccaaaacat tagttaaaga tgaaaatgaa gaagatgagg aagatgaaga cgatgacgat 600 gatgttgata gtgatccaat attagattca gaatctattc cattaagaca tactacaaat 660 agaataagag taagtcctca tgctcaacaa actggggaat acttaactgc ttcaatgtca 720 gaaaatggtg aagtttatat atttgattta ctggcacaat ataaggcatt tgacacacca 780 ggttatatga ttcctaaatc atcgaaaaga ccaattcata ctattcgtgc ccatgggaat 840 gttgaaggtt atggattaga ttggtctcca ttagtaaata caggggcttt attatctgga 900 gatatgtcag ggagaattta tttaactaat agaacgacat caagttggac cactgataaa 960 actccatttt ttgcatcaca atcttcaatt gaagatattc aatggtcaac tggtgaaact 1020 acagtgtttg ccacgggtgg atgtgatgga tatatttgta tttgggatac aagatcgaaa 1080 aaacataaac ctgcattatc agtaattgct tctaaatctg atgttaatgt gatatcttgg 1140 agttctaaaa tcaatcattt attggcatca ggacatgacg atggtagttg gggtgtatgg 1200 gatttaagaa atttcacaaa caataccacc agtaatcctt cacctgtggc taattatgat 1260 ttccataaat cgccaatcac atcaatttca ttcaatccat tagatgaatc aatcattgct 1320 gtttcatcag aagataatac tgttacatta tgggatcttg ctgttgaagc tgatgatgaa 1380 gaaatttctc aacaaagaaa agaagctcaa gaattacatg atattccacc acaattatta 1440 tttgtccatt ggcaaagaga tgttaaagat gttagatggc atccacaaat tcctggttgt 1500 ttggtatcta ctggtggtga tggattaaac atttggaaaa ctatatctgt gtaa 1554 <210> SEQ ID NO 98 <211> LENGTH: 2280 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/NM_005610.1 <309> DATABASE ENTRY DATE: 2001-12-20 <313> RELEVANT RESIDUES: (1)..(2280) <400> SEQUENCE: 98 cgcgcgcaca gagcgagctc ttgcagcctc cccgcccctc ccgcaacgct cgaccccagg 60 attcccccgg ctcgcctgcc cgccatggcc gacaaggaag cagccttcga cgacgcagtg 120 gaagaacgag tgatcaacga ggaatacaaa atatggaaaa agaacacccc ttttctttat 180 gatttggtga tgacccatgc tctggagtgg cccagcctaa ctgcccagtg gcttccagat 240 gtaaccagac cagaagggaa agatttcagc attcatcgac ttgtcctggg gacacacaca 300 tcggatgaac aaaaccatct tgttatagcc agtgtgcagc tccctaatga tgatgctcag 360 tttgatgcgt cacactacga cagtgagaaa ggagaatttg gaggttttgg ttcagttagt 420 ggaaaaattg aaatagaaat caagatcaac catgaaggag aagtaaacag ggcccgttat 480 atgccccaga acccttgtat catcgcaaca aagactcctt ccagtgatgt tcttgtcttt 540 gactatacaa aacatccttc taaaccagat ccttctggag agtgcaaccc agacttgcgt 600 ctccgtggac atcagaagga aggctatggg ctttcttgga acccaaatct cagtgggcac 660 ttacttagtg cttcagatga ccataccatc tgcctgtggg acatcagtgc cgttccaaag 720 gagggaaaag tggtagatgc gaagaccatc tttacagggc atacggcagt agtagaagat 780 gtttcctggc atctactcca tgagtctctg tttgggtcag ttgctgatga tcagaaactt 840 atgatttggg atactcgttc aaacaatact tccaaaccaa gccactcagt tgatgctcac 900 actgctgaag tgaactgcct ttctttcaat ccttatagtg agttcattct tgccacagga 960 tcagctgaca agactgttgc cttgtgggat ctgagaaatc tgaaacttaa gttgcattcc 1020 tttgagtcac ataaggatga aatattccag gttcagtggt cacctcacaa tgagactatt 1080 ttagcttcca gtggtactga tcgcagactg aatgtctggg atttaagtaa aattggagag 1140 gaacaatccc cagaagatgc agaagacggg ccaccagagt tgttgtttat tcatggtggt 1200 catactgcca agatatctga tttctcctgg aatcccaatg aaccttgggt gatttgttct 1260 gtatcagaag acaatatcat gcaagtgtgg caaatggcag agaacattta taatgatgaa 1320 gaccctgaag gaagcgtgga tccagaagga caagggtcct agatatgtct ttacttgttg 1380 tgattttaga ctcccctttt ttcttctcaa ccctgagagt gatttaacac tggttttgag 1440 acagacttta ttcagctatc cctctatata ataggtacca ccgataatgc tattagccca 1500 aaccgtgggt ttttctaaat attaataggg gggcttgatt caacaaagcc acagacttaa 1560 cgttgaaatt ttcttcagga attttctagt aacccaggtc taaagtagct acagaaaggg 1620 gaatattatg tgtgattatt tttcttctta tgctatatcc ccaagttttt cagactcatt 1680 taagtaaagg ctagagtgag taaggaatag agccaaatga ggtaggtgtc tgagccatga 1740 agtataaata ctgaaagatg tcacttttat tcaggaaata gggggagttc aagtcgtata 1800 gattcctact cgaaaatctt gacacctgac tttccaggat gcacattttc atacgtagac 1860 cagtttcctc ttggtttctt cagttaagtc aaaacaacac gttcctcttt ccccatatat 1920 tcatatattt ttgctcgtta gtgtatttct tgagctgttt tcatgttgtt tatttcctgt 1980 ctgtgaaatg gtgttttttt ttttgttgtt ggtttttttt tttttttttt aacttgggac 2040 caccaagttg taaagatgta tgtttttacc tgacagttat accacaggta gactgtcaag 2100 ttgagaagag tgaatcaata acttgtattt gttttaaaaa ttaaattaat ccttgataag 2160 agttgctttt tttttttagg agttagtcct tgaccactag tttgatgcca tctccatttt 2220 gggtgacctg tttcaccagc aggcctgtta ctctccatga ctaactgtgt aagtgcttaa 2280 <210> SEQ ID NO 99 <211> LENGTH: 1144 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <301> AUTHORS: Bauer and Burgers <302> TITLE: Molecular cloning, structure ande expression of the yeast proliferating cell nuclear antigen gene <303> JOURNAL: Nucleic Acids Research <304> VOLUME: 18 <305> ISSUE: 2 <306> PAGES: 261-265 <307> DATE: 1990 <308> DATABASE ACCESSION NUMBER: x16676 <309> DATABASE ENTRY DATE: 1993-09-30 <400> SEQUENCE: 99 acgcgtaact tttttttttt ggatttcaac tgatagtttt cgtactttgc ttcctctggt 60 acataaaatt atatataaga aacacttttg ctttagcctt cctttctttc cacttgcacc 120 tttcactttc gccgtccttt ttcactcaca gcaacaagca gcaagcacta agtacgcagt 180 caaaagagag aaaaaatgtt agaagcaaaa tttgaagaag catccctttt caagagaata 240 attgatggtt tcaaagattg tgtccagttg gtcaatttcc aatgtaaaga agatggtatc 300 attgcacaag ctgtcgatga ctcaagagtt ctattggtct ccttggaaat aggtgtcgaa 360 gccttccaag aatatagatg tgaccatcct gttacgttag gtatggatct aacctcacta 420 agtaaaatcc tacgttgtgg taacaacacc gatacattaa cactaattgc tgacaacaca 480 ccggattcca tcatcttatt atttgaggat accaagaaag accgtatagc cgaatactct 540 ctgaaattga tggatatcga tgctgatttc ttaaagattg aagaattaca gtacgactcc 600 accctgtcat tgccatcttc cgaattctct aaaattgttc gtgacttgtc ccaattgagt 660 gattctatta atatcatgat caccaaagaa acaataaagt ttgtagctga cggtgatatc 720 ggatcaggtt cagtcataat aaaaccattc gtggatatgg aacatcctga aacaagcatc 780 aaacttgaaa tggatcaacc tgtcgacttg acgttcggag ctaaatattt attggacatc 840 attaagggct cctccctttc tgatagagtt ggtatcaggc tctccagcga agctcctgct 900 ttattccaat ttgatttgaa gagtgggttc ctacagtttt tcttggctcc taaatttaat 960 gacgaagaat aaatgtaaat tatctatata gttgtatact aaaaataata aacaaaaaaa 1020 aaacagtaaa gtttgtttta aatgaaaata aataacaaag aaaataaaga ctaagtagtc 1080 agttaatatc agcatttttg tgtgacttat acagtattta tgacatatct tacattaatc 1140 taga 1144 <210> SEQ ID NO 100 <211> LENGTH: 1245 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 100 atgtcacacc aacaagaaga cgtcgtagac gatactcaag aagaatatat caatgttaat 60 gaagtggctg aggaagttgc agatgatgat caagcgccac ccgatgaaga agatgaggag 120 atggaattag atgatgagca tgagacttta gaaattgaca tgtccaacaa ttcatggact 180 tattttgata aacataccga tagtatattt actatttttt cacatcctaa attgccaatg 240 gtattgactg agggtggtga caacacggca tacttatgga ccacacacac ccaaccacca 300 agatttgttg gcgaaatcac tggacataaa gagtctgtta tatctggagg gtttactgca 360 gacggcaagt ttgttgttac tgcagacatg aatggattaa ttcaagtttt caaagccaca 420 aaaggaggtg aacagtgggt gaaatttggt gaattggacg aagttgaaga agtgttgttt 480 gttactgtgc atccaacatt accattcttt gcctttggtg ctaccgatgg atctatatgg 540 gtctaccaaa tagacgaatc cagtaaactg ctagtgcaaa ttatgtctgg gttctcacac 600 acattaaaat gtaatggtgc tgtatttata caaggaaaag atgaaaatga tttgacattg 660 gtctctataa gtgaagatgg tactgtggtg aactggaact gttttacagg acaagtgaat 720 tataaattgc aacctcatga tgactttaaa ggagttgaga gtccgtgggt cacggtcaaa 780 gtacatggta atcttgtggc cattggtggc agagatggcc agctatcaat tgtgaacaat 840 gacactggta aaatcgttca tactcttaaa acattggata atgtcgacga cattgcagaa 900 ctctcaattg aggcattgag ttggtgtgaa agcaaaaata ttaacctctt ggcagtgggt 960 ttggtttctg gtgacgttta ttatttgata ctcagcaatg gagattgaga aagaacttga 1020 aagttgacga tgccatcacc aaattacaat ttgttggcga aacccccatt ttggtgggaa 1080 atagtatgga tggtaaaatt acaaatggga acctagaact ggtgaaaaat gtttgctggt 1140 gtgggaacaa acatgggagt attggacttt gctattttag atggaggtaa aaagttggtt 1200 actgctggtg atgaaggtgt tgcattggtc tttgtacatg aatag 1245 <210> SEQ ID NO 101 <211> LENGTH: 1231 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <300> PUBLICATION INFORMATION: <301> AUTHORS: Almendral, Huebsch, Blundell, MacDonald-Bravo and Bravo <302> TITLE: Cloning and sequence of the human nuclear protein cyclin: Homology with DNA-binding protein <303> JOURNAL: Proc. Natl. Acad. Sci. U.S.A. <304> VOLUME: 84 <305> ISSUE: 6 <306> PAGES: 1575-1579 <307> DATE: 1987 <308> DATABASE ACCESSION NUMBER: M15796 <309> DATABASE ENTRY DATE: 1993-04-27 <400> SEQUENCE: 101 aggtctcagc cggtcgtcgc gacgttcgcc cgctcgctct gaggctcctg aagccgaaac 60 tagctagact ttcctccttc ccgcctgcct gtagcggcgt tgttgccact ccgccaccat 120 gttcgaggcg cgcctggtcc agggctccat cctcaagaag gtgttggagg cactcaagga 180 cctcatcaac gaggcctgct gggatattag ctccagcggt gtaaacctgc agagcatgga 240 ctcgtcccac gtctctttgg tgcagctcac cctgcggtct gagggcttcg acacctaccg 300 ctgcgaccgc aacctggcca tgggcgtgaa cctcaccagt atgtccaaaa tactaaaatg 360 cgccggcaat gaagatatca ttacactaag ggccgaagat aacgcggata ccttggcgct 420 agtatttgaa gcaccaaacc aggagaaagt ttcagactat gaaatgaagt tgatggattt 480 agatgttgaa caacttggaa ttccagaaca ggagtacagc tgtgtagtaa agatgccttc 540 tggtgaattt gcacgtatat gccgagatct cagccatatt ggagatgctg ttgtaatttc 600 ctgtgcaaaa gacggagtga aattttctgc aagtggagaa cttggaaatg gaaacattaa 660 attgtcacag acaagtaatg tcgataaaga ggaggaagct gttaccatag agatgaatga 720 accagttcaa ctaacttttg cactgaggta cctgaacttc tttacaaaag ccactccact 780 ctcttcaacg gtgacactca gtatgtctgc agatgtaccc cttgttgtag agtataaaat 840 tgcggatatg ggacacttaa aatactactt ggctcccaag atcgaggatg aagaaggatc 900 ttaggcattc ttaaaattca agaaaataaa actaagctct ttgagaactg cttctaagat 960 gccagcatat actgaagtct tttctgtcac caaatttgta cctctaagta catatgtaga 1020 tattgttttc tgtaaataac ctattttttt tctctattct ctccaatttg tttaaagaat 1080 aaagtccaaa gtctgatctg gtctagttaa cctagaagta tttttgtctc ttagaaatac 1140 ttgtgatttt tataatacaa aagggtcttg actctaaatg cagttttaag aagtgttttt 1200 gaatttaaat aaagttactt gaatttcaaa c 1231 <210> SEQ ID NO 102 <211> LENGTH: 840 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/BAA77792.1 <309> DATABASE ENTRY DATE: 1999-07-29 <313> RELEVANT RESIDUES: (1)..(840) <400> SEQUENCE: 102 atgtctgctc ccactatgag atccacctca atattgacag agcatttggg atatccgccc 60 atctcgcttg ttgatgatat cattaatgct gtaaatgaaa ttatgtacaa gtgcactgct 120 gccatggaaa aatatctgct atccaagagc aaaatcggcg aggaagatta tggagaagag 180 atcaaaagtg gagttgctaa gttggaatca cttttggaaa actccgtgga taagaatttt 240 gacaaactag aactatatgt tttgaggaac gtccttcgaa tccctgaaga gtatttggac 300 gccaatgttt ttagattgga gaaccaaaag gatctggtca ttgtagatga gaatgagttg 360 aagaaaagtg aggagaaact tcgagagaaa gtgaacgacg tggagttagc gttcaaaaag 420 aatgaaatgc tattgaaaag agttacaaaa gtgaaaagac tgttgtttac gataagagga 480 ttcaaacaaa agctaaacga gttactgaaa tgcaaagacg atgtacaatt gcagaaaatt 540 ttggagtcgt taaaacctat agatgacaca atgactctac tgactgattc attacgtaaa 600 ctatatgttg atagtgaaag taccagttca acagaggagg tagaggcact actgcagaga 660 ttgaagacca acgggaagca aaataataag gatttcagaa cacgatatat cgatataagg 720 acgaataatg tcctacgaaa attggggcta ctaggtgata aagaggacga aaaacagtct 780 gccaagccgg atgcgaggac gcaagcaggg gatatagtta gtatagatat tgaagagcct 840 <210> SEQ ID NO 103 <211> LENGTH: 945 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 103 atgtcagata aaactttaga cgaacgtact acagcaattc ttactgaaca tttagaattt 60 gctcccttga cacttattga tgacgtgatc aatgcggtga atgaaatcat gtacaaggga 120 acaacagcta ttgaaacata tttaaaagaa caaaaacaat taatgaaaaa tgggatattt 180 accaaagtta ctgaagatga aatagaaatt ggtatgggga aattagaatc attattagaa 240 tcgactatag ataagaattt tgataaattt gaattatatt gtttaagaaa tattttcaat 300 atacctaaag atctaatacc atatatacag ttaagccatc aacaaggaat tgaatttaaa 360 agtgataatg ttgaacaaaa acgtgaattt gatcaacaaa ttaaaaattt acaattgaaa 420 atcatgcaag aattacaact tcgaaaaatc ttaaaattac aacttgtcaa agtccaaaaa 480 ttaattaaag tattaatagc cattgataat gatttcaaga aaatagattt tgctagtggt 540 ggtggtggta atgaagaatc aataagaatt ttgaaaaatc ttcaacctat tgatgaaaca 600 ttatattttt taattagtca aattaaaaat ctaataaatc aaattgaaca attatcaaat 660 aaagttaata ccaatttgaa aactcaaaaa tttataccca atttgcgtga taaattcatt 720 gatggtagaa catttagagt tttacaacaa acggggattt ggaaagattt ggaaaaaaat 780 gatatcaaga ttctggtgca gggaaatgac aataataata ataataataa taataataat 840 aataccttaa cagatttaca aaatcaagac gacattgata tgataatacc agaacaagac 900 gatatagatg tggatgcaat aaagaatata aatgctcaaa tttaa 945 <210> SEQ ID NO 104 <211> LENGTH: 5718 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/AAB64747.1 <309> DATABASE ENTRY DATE: 1997-08-01 <313> RELEVANT RESIDUES: (1)..(5718) <400> SEQUENCE: 104 atgtcacatt ccggagctgc catttttgag aaagtttctg ggataattgc cataaatgag 60 gatgtttcac ccgcagaatt gacatggagg tctacggacg gtgacaaggt tcacacagtt 120 gtcttatcca ctattgacaa gttacaagct acccctgctt ccagtgaaaa aatgatgttg 180 aggctaatcg ggaaagtgga tgagtcaaaa aagagaaaag acaacgaagg aaatgaggtt 240 gtgcccaaac cgcaacgtca tatgttttcg tttaacaata gaacagttat ggataatatc 300 aagatgaccc ttcaacaaat catctcacgg tataaagatg cagatatcta cgaagaaaag 360 agaagaagag aggagtctgc gcaacacaca gaaacaccaa tgagctcttc ttctgttact 420 gcagggactc ccacaccaca tctcgataca ccacaattga ataatggggc tccgttgatt 480 aatacagcca aactagatga ttctctctct aaagaaaaat tgttgaccaa tttaaagcta 540 cagcaatctt tactgaaagg aaacaaagtt ctaatgaagg tttttcagga aacagtcatt 600 aacgccggtt tgcctccatc tgaattttgg tcaactagaa ttccgttatt gagggctttt 660 gccttatcta cttctcaaaa agttgggcct tacaacgttt tgtcaactat caagccggtg 720 gcttcatcgg aaaacaaagt caatgttaat ttgtcaagag aaaaaatttt gaatattttt 780 gagaactatc caattgtaaa gaaagcttac actgataatg tgcccaaaaa tttcaaagaa 840 ccagagttct gggcaaggtt cttctcttcg aagttattca gaaaattaag gggtgaaaag 900 atcatgcaaa atgatagagg tgacgtaatc attgacaggt acttgacatt ggatcaagag 960 ttcgacagaa aagatgatga catgctattg catcctgtga aaaaaattat agatttagat 1020 ggtaacatac aggacgaccc agttgtacga ggcaacaggc ccgacttcac tatgcagcca 1080 ggtgtggata ttaatggtaa tagcgatggt accgtggaca tcttaaaggg tatgaataga 1140 ttgagtgaaa aaatgattat ggctttgaag aatgagtatt caaggacaaa tctacagaac 1200 aaatctaata ttacaaacga tgaggaagat gaagataatg atgaaagaaa tgaactgaaa 1260 atcgatgact taaacgaaag ctacaagaca aactatgcaa tcatacatct gaaaaggaac 1320 gcacatgaaa agacaaccga caacgatgcg aaaagctcgg cagactcgat aaagaatgca 1380 gatttgaagg tttctaatca acaaatgtta caacagttgt cattggtcat ggataattta 1440 attaataagc tagacttgaa ccaagtagtt cctaacaacg aagtcagcaa caagatcaat 1500 aaaagagtca taactgcaat caagattaac gccaaacagg ctaagcataa caatgttaat 1560 tcagcactcg gctcttttgt cgacaacact tctcaagcaa atgaattaga ggtgaaaagt 1620 accctaccaa tagacctatt agaaagttgt agaatgctac acacaacgtg ctgtgaattt 1680 ctaaagcact tttatattca ttttcagagc ggtgaacaaa agcaagccag taccgtcaaa 1740 aaactttata atcatttgaa ggactgtatt gaaaagctga atgagctatt tcaagacgtc 1800 cttaatggtg atggtgaatc tatgtcaaac acatgtaccg cctatttgaa gccagttttg 1860 aactccatta ctttggctac tcataagtac gatgagtact tcaacgaata taacaacaat 1920 tcgaactagg atgtttcacc cgcagaattg acatggaggt ctacggacgg tgacaaggtt 1980 cacacagttg tcttatccac tattgacaag ttacaagcta cccctgcttc cagtgaaaaa 2040 atgatgttga ggctaatcgg gaaagtggat gagtcaaaaa agagaaaaga caacgaagga 2100 aatgaggttg tgcccaaacc gcaacgtcat atgttttcgt ttaacaatag aacagttatg 2160 gataatatca agatgaccct tcaacaaatc atctcacggt ataaagatgc agatatctac 2220 gaagaaaaga gaagaagaga ggagtctgcg caacacacag aaacaccaat gagctcttct 2280 tctgttactg cagggactcc cacaccacat ctcgatacac cacaattgaa taatggggct 2340 ccgttgatta atacagccaa actagatgat tctctctcta aagaaaaatt gttgaccaat 2400 ttaaagctac agcaatcttt actgaaagga aacaaagttc taatgaaggt ttttcaggaa 2460 acagtcatta acgccggttt gcctccatct gaattttggt caactagaat tccgttattg 2520 agggcttttg ccttatctac ttctcaaaaa gttgggcctt acaacgtttt gtcaactatc 2580 aagccggtgg cttcatcgga aaacaaagtc aatgttaatt tgtcaagaga aaaaattttg 2640 aatatttttg agaactatcc aattgtaaag aaagcttaca ctgataatgt gcccaaaaat 2700 ttcaaagaac cagagttctg ggcaaggttc ttctcttcga agttattcag aaaattaagg 2760 ggtgaaaaga tcatgcaaaa tgatagaggt gacgtaatca ttgacaggta cttgacattg 2820 gatcaagagt tcgacagaaa agatgatgac atgctattgc atcctgtgaa aaaaattata 2880 gatttagatg gtaacataca ggacgaccca gttgtacgag gcaacaggcc cgacttcact 2940 atgcagccag gtgtggatat taatggtaat agcgatggta ccgtggacat cttaaagggt 3000 atgaatagat tgagtgaaaa aatgattatg gctttgaaga atgagtattc aaggacaaat 3060 ctacagaaca aatctaatat tacaaacgat gaggaagatg aagataatga tgaaagaaat 3120 gaactgaaaa tcgatgactt aaacgaaagc tacaagacaa actatgcaat catacatctg 3180 aaaaggaacg cacatgaaaa gacaaccgac aacgatgcga aaagctcggc agactcgata 3240 aagaatgcag atttgaaggt ttctaatcaa caaatgttac aacagttgtc attggtcatg 3300 gataatttaa ttaataagct agacttgaac caagtagttc ctaacaacga agtcagcaac 3360 aagatcaata aaagagtcat aactgcaatc aagattaacg ccaaacaggc taagcataac 3420 aatgttaatt cagcactcgg ctcttttgtc gacaacactt ctcaagcaaa tgaattagag 3480 gtgaaaagta ccctaccaat agacctatta gaaagttgta gaatgctaca cacaacgtgc 3540 tgtgaatttc taaagcactt ttatattcat tttcagagcg gtgaacaaaa gcaagccagt 3600 accgtcaaaa aactttataa tcatttgaag gactgtattg aaaagctgaa tgagctattt 3660 caagacgtcc ttaatggtga tggtgaatct atgtcaaaca catgtaccgc ctatttgaag 3720 ccagttttga actccattac tttggctact cataagtacg atgagtactt caacgaatat 3780 aacaacaatt cgaactagat ggaactagag cccactcttt ttggtataat agaggcattg 3840 gctcctcaat tattgtcgca gagtcatttg cagacatttg tatctgatgt agtcaattta 3900 ctgcgatcat ccaccaaatc ggcaactcaa ttaggccctt taattgattt ttacaaatta 3960 caatcactag attcgcctga aacaacaatt atgtggcata aaattgagaa atttctcgat 4020 gctttatttg gaatccagaa caccgatgat atggtaaagt acctctctgt ctttcaatct 4080 ttgcttccat caaattacag agcaaaaatt gtccaaaaat catctgggct caatatggag 4140 aaccttgcta accatgaaca tttacttagc ccagtgcggg ctccaagtat atatacagaa 4200 gcttcatttg aaaacatgga ccgattttct gaaagaaggt ccatggtatc ttcgcctaat 4260 cgttacgttc cctcttcaac ctacagttct gttactttga gacagttgtc aaatccttat 4320 tatgtgaaca ctatacccga ggaagatatc ctaaaatacg tatcatatac attattagct 4380 acgacatcgg cactatttcc gtttgatcat gagcaaatac aaattccgtc taagataccc 4440 aattttgaga gtggactttt acatttaata tttgaagcgg gtttattata tcaaagtttg 4500 ggttataaag tggagaagtt taggatgttg aatatatctc caatgaaaaa agcattgatt 4560 atagaaattt cagaagaatt acaaaactac acagcatttg tgaacaatct ggtctcttca 4620 gggacagtag tgtcattgaa atcgttatat cgtgaaatat atgaaaatat aataaggctt 4680 cgaatatact gtaggtttac agaacacctt gaagaattga gcggagatac attcttgatt 4740 gaattaaata ttttcaaatc ccacggagat cttactataa gaaaaatagc aacgaatttg 4800 tttaattcaa tgatttctct ttattatgag tatttaatga attggttgac taaaggtcta 4860 ctccgagcta cttatggaga attcttcatt gctgaaaaca ctgatacaaa tggtacagac 4920 gatgatttta tttaccacat tcctatagag ttcaaccaag aaagagttcc ggccttcata 4980 ccgaaagagt tggcatataa aatattcatg atcggcaaat cgtatatctt cctagaaaag 5040 tactgtaaag aggttcaatg gacaaacgaa ttttctaaaa agtatcatgt cctgtaccag 5100 agcaattctt atcggggaat atcaacgaac ttttttgaaa ttataaatga tcaatattct 5160 gaaattgtta atcatactaa tcaaattcta aatcagaagt ttcattacag agacgtggta 5220 tttgcgttaa agaatattct tctcatgggt aaatctgatt ttatggatgc tcttatagaa 5280 aaggccaatg atattctcgc gacaccatcg gattcattgc caaattataa gttaacaagg 5340 gttttacagg aagccgtgca gctttcttcc ttaagacatt taatgaatag tccccgtaat 5400 agttctgtca ttaatggatt ggatgcgagg gtactcgatc ttggacatgg atccgtgggt 5460 tgggatgttt ttactttaga ttacatcctc tacccccctt tgagtttagt attaaacgta 5520 aatcgtcctt ttggcaggaa agagtatcta cgaattttca attttttatg gagatttaaa 5580 aagaacaatt atttctatca aaaggaaatg ttgaagagta atgatataat cagatcattc 5640 aagaaaatca gaggttacaa cccgctcatc cgtgatatta tcaataaact ttctagaatc 5700 agtatactta gaactcaa 5718 <210> SEQ ID NO 105 <211> LENGTH: 2082 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 105 atggatataa ttagaggtgc atgttcagtt gataaaattg gggggatggt gtatattaga 60 gaagatttag caccgctgat gttggaatgg aaaccaattg atgaacaaga agaagataga 120 gcaatttcaa tcccattgaa ttctttaact acattacaaa gtaccaaaga aacctcaccg 180 aaaatgatac taaaaattgt atacaaacta acatctggtc cacctaatac aaatgcagat 240 ggaactgaca atggtggtgg tggtggtggt gaacaaaaat catttaaatt gacatttact 300 aatagaccaa ccatgaacac tattaaagat tctctacaaa caattgttgc tagatcaaga 360 actaagggtt tgaaggtacc agtactccaa ctccagctcc agcaccagct tcaacatttg 420 gggtcagcac cacaagctga ttctaccaga gattcgacat catcatcaac accaatacca 480 cctacaacat ctggaacttc tactagttca tcattattat cattagcagc atcacaatca 540 ttatctgatg caaatttatt gaaaaatttc gaactacagc aaaaactttt attagaagat 600 cgtcaattac gtgatgtttt cactaaatca gtcatgcaat ttaaattatc tcctcaagta 660 ttttggtcat caagattaaa tcaattacga acatttgctt tgacaatatc tcaacataaa 720 ggtccatata atgtattgag tacaattaaa ccggtggcca cttctgataa tcaagtgaat 780 gttaatgtta cgcgtgatac cattaatgaa atatttacta tttaccccat cataaagaaa 840 gcatttgatg atttggttcc taacaagttt aatgaaggag aattttggtc gagatttttc 900 aattctaaat tgtttagacg cttaagaggt gataaaatca gtattagtaa tagtcgagga 960 gatgttgtat tggacaaata tttgtatata gatcaaaact atcaagaaaa attacaaaaa 1020 tcatctactt tggaaaacaa cggttctggt ggtggtggtg gtggcgctgg tggtggtagt 1080 ggtaattcag aacaaggaat acaaacattg gaatctccac atgttaaaaa atttcttgat 1140 ttgatgggaa atcaacaaga taattcacaa aaattgggga atagaccaga ttttactatg 1200 agatatgatg aagacaccaa tgtagatgat gataataaaa aacctacttt aggaaatgaa 1260 aatgaaatga ttatattgat gaaaaatatg aatcgattat cgtcgaaaat gatgagtatg 1320 agttctacta atggaccaga gaaaccttca gaaactacaa ttgatggatt atctgctgct 1380 gaattgaatg aatatgaaga agaattagat ttgcatgatt taaatgattc agaaaattta 1440 caatatataa aattaaacat taatactgat attgccaagg gaacaaaact tgattcatat 1500 gaaggatcaa atactaataa caagatttct caagatgaat tacataaata tttacaatct 1560 caaactttcc aaggacaaat agaattaaca gaaacttata cttgtaaaag tgaagaaatt 1620 gaaaaaacct ccatggaaat agccatgctt attaaacaaa atttccgaac atttaaatta 1680 attaataaag aaaatgatat tgcggggaca aacattgttc ctaattcatt aatacaagaa 1740 atcattactt ataatattac gatagttgaa tttttatctc atttttggaa gattttttta 1800 catgggaata atcctggtca attaaagaaa attttcacca gtttgaaaaa ttgtcaatct 1860 ggtttaatag aattagaaaa taaagcgatt gatcaattca aatctatgga tatattacaa 1920 aaaaatcaaa aattacaaga taaagtttta aaagattttg catcatgtct tcaacccatg 1980 aaaatagcat tagataaagc atgtaatgaa tatgttgaag cagtaaagaa agctaaacct 2040 gaattaaatg aaaatggtaa acgtcctcta ccagaggagt ga 2082 <210> SEQ ID NO 106 <211> LENGTH: 466 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: (1)..(466) <223> OTHER INFORMATION: n is unknown <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/W19128 <309> DATABASE ENTRY DATE: 1996-05-03 <313> RELEVANT RESIDUES: (1)..(466) <400> SEQUENCE: 106 ngncacattc tgcnnagaga tcctttgacc ctgnatncag ccgatccctg tgaaaataat 60 gggantggaa aaaacgtgtc cagnattcct tctctgtcat gtngtgggna acattttctg 120 catatttcat tttnactgct ggataggtcc tnaatatgga ctcaatgata ncagaagtta 180 aattatatct tagaccgtta nagccatcag tttggggccg gacatcagcn agaaatgcag 240 caganatgcc aanatcctgc ttatgattgg atntggaaga actatctgtt gcattcacat 300 ttaaaccgat tggnccagaa ttcctcagca ctgatcactt gactcacgaa caaggtcttt 360 ataaagctga aacaaaacca ggatcttctt gcagcattct gttcatnccc tccagtncct 420 gnatttgcnt tccncttgaa tttgggcagc anctgctgan gaaggt 466 <210> SEQ ID NO 107 <211> LENGTH: 2460 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/CAA96007.1 <309> DATABASE ENTRY DATE: 1997-08-11 <313> RELEVANT RESIDUES: (1)..(2460) <400> SEQUENCE: 107 atggaactag agcccactct ttttggtata atagaggcat tggctcctca attattgtcg 60 cagagtcatt tgcagacatt tgtatctgat gtagtcaatt tactgcgatc atccaccaaa 120 tcggcaactc aattaggccc tttaattgat ttttacaaat tacaatcact agattcgcct 180 gaaacaacaa ttatgtggca taaaattgag aaatttctcg atgctttatt tggaatccag 240 aacaccgatg atatggtaaa gtacctctct gtctttcaat ctttgcttcc atcaaattac 300 agagcaaaaa ttgtccaaaa atcatctggg ctcaatatgg agaaccttgc taaccatgaa 360 catttactta gcccagtgcg ggctccaagt atatatacag aagcttcatt tgaaaacatg 420 gaccgatttt ctgaaagaag gtccatggta tcttcgccta atcgttacgt tccctcttca 480 acctacagtt ctgttacttt gagacagttg tcaaatcctt attatgtgaa cactataccc 540 gaggaagata tcctaaaata cgtatcatat acattattag ctacgacatc ggcactattt 600 ccgtttgatc atgagcaaat acaaattccg tctaagatac ccaattttga gagtggactt 660 ttacatttaa tatttgaagc gggtttatta tatcaaagtt tgggttataa agtggagaag 720 tttaggatgt tgaatatatc tccaatgaaa aaagcattga ttatagaaat ttcagaagaa 780 ttacaaaact acacagcatt tgtgaacaat ctggtctctt cagggacagt agtgtcattg 840 aaatcgttat atcgtgaaat atatgaaaat ataataaggc ttcgaatata ctgtaggttt 900 acagaacacc ttgaagaatt gagcggagat acattcttga ttgaattaaa tattttcaaa 960 tcccacggag atcttactat aagaaaaata gcaacgaatt tgtttaattc aatgatttct 1020 ctttattatg agtatttaat gaattggttg actaaaggtc tactccgagc tacttatgga 1080 gaattcttca ttgctgaaaa cactgataca aatggtacag acgatgattt tatttaccac 1140 attcctatag agttcaacca agaaagagtt ccggccttca taccgaaaga gttggcatat 1200 aaaatattca tgatcggcaa atcgtatatc ttcctagaaa agtactgtaa agaggttcaa 1260 tggacaaacg aattttctaa aaagtatcat gtcctgtacc agagcaattc ttatcgggga 1320 atatcaacga acttttttga aattataaat gatcaatatt ctgaaattgt taatcatact 1380 aatcaaattc taaatcagaa gtttcattac agagacgtgg tatttgcgtt aaagaatatt 1440 cttctcatgg gtaaatctga ttttatggat gctcttatag aaaaggccaa tgatattctc 1500 gcgacaccat cggattcatt gccaaattat aagttaacaa gggttttaca ggaagccgtg 1560 cagctttctt ccttaagaca tttaatgaat agtccccgta atagttctgt cattaatgga 1620 ttggatgcga gggtactcga tcttggacat ggatccgtgg gttgggatgt ttttacttta 1680 gattacatcc tctacccccc tttgagttta gtattaaacg taaatcgtcc ttttggcagg 1740 aaagagtatc tacgaatttt caatttttta tggagattta aaaagaacaa ttatttctat 1800 caaaaggaaa tgttgaagag taatgatata atcagatcat tcaagaaaat cagaggttac 1860 aacccgctca tccgtgatat tatcaataaa ctttctagaa tcagtatact tagaactcaa 1920 ttccagcaat tcaactcgaa gatggaatct tattatttga actgcattat agaggaaaat 1980 tttaaagaaa tgacccggaa actgcaacgc acagagaata aaagccaaaa ccaattcgac 2040 ttaattagat taaataatgg caccatagaa ttaaatggga ttttaacccc aaaagctgaa 2100 gtactaacaa agtcttcaag cagtaaaccc caaaaacacg caatcgaaaa gacgctgaat 2160 attgatgaat tagaaagtgt acataacacg ttcttgacga atattctttc tcataagctt 2220 tttgcaacta acacaagtga aataagcgtt ggtgattatt ctgggcaacc atacccaact 2280 tcattggttt tacttttaaa ttcggtttac gagttcgtca aagtttattg taatttgaac 2340 gacattggat acgaaatctt cattaaaatg aatctcaatg atcacgaagc atctaacgga 2400 ttattgggaa aatttaatac gaatttaaag gaaattgtta gccagtataa aaattttaaa 2460 <210> SEQ ID NO 108 <211> LENGTH: 1921 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 108 atggcgttaa acaaggtaca actaataaaa ttatattcca atcgattagt gaaatcattg 60 gttcctgtgg aattcggtga ggcattcatc caaagtataa tcaatgactt gcaaaccact 120 ttactaaata cttcttctga agaacaaaat ttgtcaataa ttataaacaa gcttaaaatg 180 caatttttaa gtaacaattt aaaaaatgaa tgggtcgaat ttcaaaacat tgttaattca 240 ttaagcaaat tcaagtcgtt ggatcagatt tgtaattatc tcgcatttct tgatgcttta 300 agagatgaga aaccagaaga tatattatca acatcaacag cgagcttgtc tcccggtaag 360 caaaatgtaa tgatcaatac ggtaaacaca gcattgacgt tatcacagtt aatcgagcct 420 tactatgata ctttatcgga acaaaccatt ttaacctact taccctacac gatgttaggt 480 ctggattcca aaatattcac cttcagcaat aattatacac gattggagat accgaaagat 540 ataaacaaca gtttcagctc attgctacgc gaagtttttg agtttgcaat actatataaa 600 caattggcaa ttgttgttga taggtataaa ggaactttag tactggccat aaagacagct 660 tacatagcaa tactagaggc tcaattgaac aaatatgtga atgatattaa caatatcttc 720 aataataaac cgaattccat attagttgtt tacaattcca ttttcccctg gatatctata 780 ctacgatttt tatatcgagt ctcaaacaga ctaaacagat tagatggtta tgaatttctc 840 acatttattt atagtttcac caaccatgga gatcccaaaa tacggggcat tgctgtgact 900 gcattcaccg aggttgtcaa accgtattat aatattgtgg aacattggat agtgaaaggg 960 gagttgattg ataataataa cgagtttttc attatctttg atcaagagca gaatgaattc 1020 aatagtataa ttaaattatt gcccaaaaaa ataccagcct ttattaaatc gagtgataaa 1080 atatttcaga ttgggaaaac attaattttt ctaaataaat attgtcgtga actaaaatgg 1140 gtaaatcagt ataacgtgaa atattctgct atattgttca ataaccatca aggcttggca 1200 tccatgacaa caaatgaaat gatcaaattg attgatctgc aatataatga gatattaacg 1260 tttctcaccc aaataatcca aggaaacaat aaattgttta ctcatgttta taatttcaag 1320 aggttttatt ttatggagac caatgatttt attgatgcga ttatggtgaa agggaaggac 1380 gtttttaatg agtcttctgt taatatttca tcaacctatc ttaggaaagt cttacaagac 1440 gctatacaaa tttcgtcggt gaaaaatttt gagtatgttg acagactcga ttcgagagtg 1500 ttgaatcccc aacacgggaa tttgggctgg gaatcgttca ccattgaata caaaattgat 1560 gatcttccca tgagttattt atttgaaggt caccaacatt tacaatattt aaaaatgttt 1620 cattttctat ggaaattaag acaattgaat aatttattaa attggcattt tgagatgttt 1680 aatgagttga atcataatgt ggtgacgaag ttgtcaagca gaaatagaag acctttggcg 1740 aaatcattga gcataatcac cagtataaga ttccatttta cccagtttct taacgaacta 1800 atagcttatt tgtcttatga tgttattgaa gaaaattttc gacagactgt atatttttag 1860 ggcagattta aagaacgatg gcgatgaaga gcttttctta ttgagcaaat cgctccgtta 1920 a 1921 <210> SEQ ID NO 109 <211> LENGTH: 3829 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/AF042378.1 <309> DATABASE ENTRY DATE: 1998-05-07 <313> RELEVANT RESIDUES: (1)..(3829) <400> SEQUENCE: 109 caggaagggc gcgggccgcg gtccctgcgc gtgcggcggc agtggcggct ctgcccggac 60 caccgtgcac ggctccgggc gaggatggcg accccggacc agaagtcgcc gaacgttctg 120 ctgcagaacc tgtgctgcag gatcctgggc aggagcgaag ctgatgtagc ccagcagttc 180 cagtatgctg tgcgggtgat tggcagcaac ttcgccccaa ctgttgaaag agatgaattt 240 ttagtagctg aaaaaatcaa gaaagagctt attcgacaac gaagagaagc agatgctgca 300 ttattttcag aactccacag aaaacttcat tcacagggag ttttgaaaaa taaatggtca 360 atactctacc tcttgctgag cctcagtgag gacccacgca ggcagccaag caaggtttct 420 agctatgcta cgttatttgc tcaggcctta ccaagagatg cccactcaac cccttactac 480 tatgccaggc ctcagaccct tcccctgagc taccaagatc ggagtgccca gtcagcccag 540 agctccggca gcgtgggcag cagtggcatc agcagcattg gcctgtgtgc cctcagtggc 600 cccgcgcctg cgccacaatc tctcctccca ggacagtcta atcaagctcc aggagtagga 660 gattgccttc gacagcagtt ggggtcacga ctcgcatgga ctttaactgc aaatcagcct 720 tcttcacaag ccactacctc aaaaggtgtc cccagtgctg tgtctcgcaa catgacaagg 780 tccaggagag aaggggatac gggtggtact atggaaatta cagaagcagc tctggtaagg 840 gacattttgt acgtctttca gggcatagat ggcaaaaaca tcaaaatgaa caacactgaa 900 aattgttaca aagtagaagg aaaggcaaat ctaagtaggt ctttgagaga cacagcagtc 960 aggctttctg agttgggatg gttgcataat aaaatcagaa gatacacgga ccagaggagc 1020 ctggaccgct cattcggact cgtcgggcag agcttttgtg ctgccttgca ccaggaactc 1080 agagaatact atcgattgct ctctgtttta cattctcagc tacaactaga ggatgaccag 1140 ggtgtgaatt tgggacttga gagtagttta acacttcggc gcctcctggt ttggacctat 1200 gatcccaaaa tacgactgaa gacccttgcg gccctagtgg accactgcca aggaaggaaa 1260 ggaggtgagc tggcctcagc tgtccacgcc tacacaaaaa caggagaccc gtacatgcgg 1320 tctctggtgc agcacatcct cagcctcgtg tctcatcctg ttttgagctt cctgtaccgc 1380 tggatatatg atggggagct tgaggacact taccacgaat tttttgtagc atcagatcca 1440 acagttaaaa cagatcgact gtggcacgac aagtatactt tgaggaaatc gatgattcct 1500 tcgtttatga cgatggatca gtctaggaag gtccttttga taggaaaatc aataaatttc 1560 ttgcaccaag tttgtcatga tcagactccc actacaaaga tgatagctgt gaccaagtct 1620 gcagagtcac cccaggacgc tgcagaccta ttcacagact tggaaaatgc atttcagggg 1680 aagattgatg ctgcttattt tgagaccagc aaatacctgt tggatgttct caataaaaag 1740 tacagcttgc tggaccacat gcaggcaatg aggcggtacc tgcttcttgg tcaaggagac 1800 tttataaggc acttaatgga cttgctaaaa ccagaacttg tccgtccagc tacgactttg 1860 tatcagcata acttgactgg aattctagaa accgctgtca gagccaccaa cgcacagttt 1920 gacagtcctg agatcctgcg aaggctggac gtgcggctgc tggaggtctc tccaggtgac 1980 actggatggg atgtcttcag cctcgattat catgttgacg gaccaattgc aactgtgttt 2040 actcgagaat gtatgagcca ctacctaaga gtatttaact tcctctggag ggcgaagcgg 2100 atggaataca tcctcactga catacggaag ggacacatgt gcaatgcaaa gctcctgaga 2160 aacatgccag agttctccgg ggtgctgcac cagtgtcaca ttttggcctc tgagatggtc 2220 catttcattc atcagatgca gtattacatc acatttgagg tgcttgaatg ttcttgggat 2280 gagctttgga acaaagtcca gcaggcccag gatttggatc acatcattgc tgcacacgag 2340 gtgttcttag acaccatcat ctcccgctgc ctgctggaca gtgactccag ggcactttta 2400 aatcaactta gagctgtgtt tgatcaaatt attgaacttc agaatgctca agatgcaata 2460 tacagagctg ctctggaaga attgcagaga cgattacagt ttgaagagaa aaagaaacag 2520 cgtgaaattg agggccagtg gggagtgacg gcagcagagg aagaggagga aaataagagg 2580 attggagaat ttaaagaatc tataccaaaa atgtgctcac agttgcgaat attgacccat 2640 ttctaccagg gtatcgtgca gcagtttttg gtgttactga cgaccagctc tgacgagagt 2700 cttcggtttc ttagcttcag gctggacttc aacgagcatt acaaagccag ggagcccagg 2760 ctccgtgtgt ctctgggtac cagggggcgg cgcagctccc acacgtgaag ctcgcggtcc 2820 tcccagggag ctgcgggtga tgttcgttgc actgctagac acgaaattcc cattgacgtc 2880 ctgcaggaac tgcatgctgc aggtgtcctg cccttccgcc cacgagtgcg ccatgtttca 2940 gcggagcggc gtgtgggaga agccacgtcg tgtttcacat gtcggagtcg aatgcatttg 3000 taaatcccta agtcaagtag gctggctgca ctgttcacat ttgtctctaa aagtcttcat 3060 cgctaaaaga taccataatt tgctgaggct tcttaagctt tctatgttat aatttatatt 3120 tgtcacttta aaaaatccat ttcttttaga aaaaattagg gtgataggat attcattagt 3180 taagatggta acgtcattgc tattttttta acatcctctt tagaggtaat ttttgttaac 3240 ataaccaaaa attaaattga aacaaaatgt cccaactaag aaaatatata gagcatttta 3300 ttttttttta gtgttgtaaa atattaacct ctgtgagatc ctttgtatct taatgcatta 3360 cctttacaca tatttattct tattttctct cctttcagag tttacatttt tatatttaat 3420 ttactatttc agatttttaa aatagtatag aaaaaagtag gagtgataga gaacaaaaat 3480 actcttatac agtgcaaccc aaataccgcg aatgcatcag ctaaagcagc gtgtaaatag 3540 gagtgatgag aaagttaatg gagtatttta ttttcaaagt tcctgataag cattggaaag 3600 aaatcgacat ggataatgaa gatttccttt ttccttgcct attttttcat tgtaaatatt 3660 tatatactac tgaccaagat gttggggtgg gggggattgt tttttgtaaa aatgtcatta 3720 tcaggtcaca taaatctgcc tttatgttgc ataagtgaaa atttagaaaa ttaaaagcaa 3780 ttatctttca aaaaaaatgg aataaattgc ttttctacat aaaaaaaaa 3829 <210> SEQ ID NO 110 <211> LENGTH: 1560 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/AAB64735.1 <309> DATABASE ENTRY DATE: 1997-08-01 <313> RELEVANT RESIDUES: (1)..(1560) <400> SEQUENCE: 110 atggaaaaat cactagcgga tcaaatttcc gatatcgcca ttaaaccggt caataaagac 60 ttcgatattg aagatgagga aaatgcatct ttatttcaac acaatgaaaa aaatggagaa 120 agtgatttaa gcgactatgg aaatagcaac acagaagaaa ccaagaaggc gcactatttg 180 gaggtggaaa agtctaagtt aagagcagaa aaaggtttag aactaaacga tccaaaatat 240 acaggtgtta aaggttcaag acaagcatta tatgaagaag tttccgagaa tgaggacgaa 300 gaagaagaag aagaagagga agaagaaaaa gaggaagatg ctctttcatt caggacagat 360 tctgaagatg aagaagtaga gattgatgaa gaagaatcag acgcggacgg cggtgaaacg 420 gaggaggctc aacagaaaag gcatgcacta tcgaaactaa ttcaacaaga gactaaacaa 480 gctattaaca aactgtctca atcagttcaa agagatgctt cgaagggtta ttccatttta 540 caacagacaa aattatttga caacatcatt gatttgagaa taaaactaca aaaagctgta 600 attgcagcaa ataagctccc attaactaca gagtcctggg aagaggctaa aatggatgat 660 tcagaggaaa caaagcgttt gctgaaggaa aacgaaaaac tgttcaataa tttattcaat 720 cggttgataa atttcagaat aaaattccaa cttggcgatc atatcactca aaatgaagag 780 gtggcgaagc ataaattgtc caaaaaaaga tctctcaaag agctttacca agaaactaat 840 agcttagact cagaactaaa agagtacagg actgccgtat taaacaagtg gtctaccaaa 900 gtttcttctg catcaggtaa cgctgcttta tcatctaaca aattcaaagc tatcaactta 960 cctgcagatg tacaagtcga aaaccaatta tccgatatgt cccgtttgat gaaaagaaca 1020 aagttgaaca ggagaaacat aacgcctttg tatttccaaa aagactgtgc taatggcagg 1080 ctaccagaat tgatttctcc cgttgtcaaa gatagtgttg atgacaatga gaattcggat 1140 gatgggcttg atatcccgaa aaactatgac ccaagaagaa aggataacaa tgccattgac 1200 attaccgaaa acccatatgt ttttgatgac gaagattttt accgtgtttt actaaacgat 1260 ttaattgaca aaaagatttc caacgctcac aattctgaaa gtgcagcaat tacaatcacc 1320 tcaactaatg ctcgttcgaa caacaagcta aagaagaata tcgatactaa ggcttccaag 1380 ggtaggaaat tgaactactc agttcaagat ccaattgcga attatgaagc ccccatcaca 1440 tccggataca aatggtcaga cgaccaaatc gatgaattct ttgcgggatt gttaggtcaa 1500 cgagtgaact ttaatgaaaa tgaggatgag gaacaacatg ccagaataga aaatgacgaa 1560 <210> SEQ ID NO 111 <211> LENGTH: 1596 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 111 atgagcttct tcggcttaca ctttcaactt aattcattga cattgaacat ttcaaatatg 60 gcaaaaaagt ctttatcaga gcaaatttct agtttatata caccaaagac tgattatgat 120 attgaggatc atgatttaga tgtatctaaa gacaatggca tttttcagca tcatgacggt 180 ggttctgaaa acgaatctga agacgaggat actggcttaa gaaatgagca ttatgttgaa 240 tcttcaaaat caaagttgag acaacagaat gaaggtgtga acttggggga aaaatacgtg 300 ggcaatgtca caagcagaag caaattgtat gacgatgagg atgacaaaca accaacagaa 360 gctagctccg gagaggagtt agatgctgaa tcagcggaag aagaagagga tgaagaatct 420 gaagatgtag cagatgatga tgaagatgac caagagtcag atcgcagtag ctcaagtgat 480 gcagagaatg acgaggacga gaacatttca cacaaaaggg aattattaaa acaattaatg 540 agcaaagaga gaagtcacat cgttaacaga ttatcccaat cagcaacaaa tgatgcatta 600 aaaggttatt caatacaaca gcaaaacaaa acttttgaaa aaatcattga tgtgaggttg 660 aaatttcaga aatcggtaac ttcaagtaat atgttaccta taaatacaag tacatattca 720 gaaaccaaat ctgaagatag cgatgaatta gtgactaaag ccaagaaaca attgtatagt 780 ttgttggatc atttattcac acttagaaac gaactagacg aaagtacctc agtcaagacc 840 cccaaaaaac gatcatttgc taaatattcg gaggttacat ctgctgcaga tgcacaattg 900 aattcccgtc gtaaccaaat attaaccaag tggtcagcta aagttgccaa ttcatccggt 960 agaaatgcca tgaatgctaa taaattcaaa actataaacc aatcttttga acaacaggtt 1020 aacaacaact tgtctgacat ggatagatta atcaaaagaa caaaattgaa ccgaagaaac 1080 gtaactccca ttggttatac caccaaagag gaggatgatc atgaaaatgg caataaaaac 1140 aaatctatcg acgaggacga cgacgatatt cccgaagata cttctgttcg taagaaaacc 1200 caaggcttgg aaaatgatta tatatttgat gacgaagatt tctatagagt attgttgaat 1260 gatttagtcg acaagaaagt gcaaacaagt gatccaacat caggtataac tatcagttta 1320 agagctgctc aaaagtccaa taaattgaaa aataatgttg atacaaaagc atctaaaggt 1380 aggaaattga gatatcacgt gcaagaacca attgctaatt ttgaaacttc aagaggcagc 1440 tggagatgga atgatgatca aattgacgag tttttcgcat ctttattggg ccaaaaggtc 1500 aatatgaatg agatagatga tgaacaagaa gaagaacaag agaatgatga taatgatatt 1560 attccagagg ataacggaat ccagttgttt ggttaa 1596 <210> SEQ ID NO 112 <211> LENGTH: 2444 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/NM_000055 <309> DATABASE ENTRY DATE: 2001-02-03 <313> RELEVANT RESIDUES: (1)..(2444) <400> SEQUENCE: 112 agtaacagtt gattgttaca ttcagtaaca ctgaatgtca gtgcagtcca atttacaggc 60 tggagcagca gctgcatcct gcatttcccc gaagtattac atgattttca ctccttgcaa 120 actttaccat ctttgttgca gagaatcgga aatcaatatg catagcaaag tcacaatcat 180 atgcatcaga tttctctttt ggtttctttt gctctgcatg cttattggga agtcacatac 240 tgaagatgac atcataattg caacaaagaa tggaaaagtc agagggatga acttgacagt 300 ttttggtggc acggtaacag cctttcttgg aattccctat gcacagccac ctcttggtag 360 acttcgattc aaaaagccac agtctctgac caagtggtct gatatttgga atgccacaaa 420 atatgcaaat tcttgctgtc agaacataga tcaaagtttt ccaggcttcc atggatcaga 480 gatgtggaac ccaaacactg acctcagtga agactgttta tatctaaatg tatggattcc 540 agcacctaaa ccaaaaaatg ccactgtatt gatatggatt tatggtggtg gttttcaaac 600 tggaacatca tctttacatg tttatgatgg caagtttctg gctcgggttg aaagagttat 660 tgtagtgtca atgaactata gggtgggtgc cctaggattc ttagctttgc caggaaatcc 720 tgaggctcca gggaacatgg gtttatttga tcaacagttg gctcttcagt gggttcaaaa 780 aaatatagca gcctttggtg gaaatcctaa aagtgtaact ctctttggag aaagtgcagg 840 agcagcttca gttagcctgc atttgctttc tcctggaagc cattcattgt tcaccagagc 900 cattctgcaa agtggatcct ttaatgctcc ttgggcggta acatctcttt atgaagctag 960 gaacagaacg ttgaacttag ctaaattgac tggttgctct agagagaatg agactgaaat 1020 aatcaagtgt cttagaaata aagatcccca agaaattctt ctgaatgaag catttgttgt 1080 cccctatggg actcctttgt cagtaaactt tggtccgacc gtggatggtg attttctcac 1140 tgacatgcca gacatattac ttgaacttgg acaatttaaa aaaacccaga ttttggtggg 1200 tgttaataaa gatgaaggga cagctttttt agtctatggt gctcctggct tcagcaaaga 1260 taacaatagt atcataacta gaaaagaatt tcaggaaggt ttaaaaatat tttttccagg 1320 agtgagtgag tttggaaagg aatccatcct ttttcattac acagactggg tagatgatca 1380 gagacctgaa aactaccgtg aggccttggg tgatgttgtt ggggattata atttcatatg 1440 ccctgccttg gagttcacca agaagttctc agaatgggga aataatgcct ttttctacta 1500 ttttgaacac cgatcctcca aacttccgtg gccagaatgg atgggagtga tgcatggcta 1560 tgaaattgaa tttgtctttg gtttacctct ggaaagaaga gataattaca caaaagccga 1620 ggaaattttg agtagatcca tagtgaaacg gtgggcaaat tttgcaaaat atgggaatcc 1680 aaatgagact cagaacaata gcacaagctg gcctgtcttc aaaagcactg aacaaaaata 1740 tctaaccttg aatacagagt caacaagaat aatgacgaaa ctacgtgctc aacaatgtcg 1800 attctggaca tcattttttc caaaagtctt ggaaatgaca ggaaatattg atgaagcaga 1860 atgggagtgg aaagcaggat tccatcgctg gaacaattac atgatggact ggaaaaatca 1920 atttaacgat tacactagca agaaagaaag ttgtgtgggt ctctaattaa tagatttacc 1980 ctttatagaa catattttcc tttagatcaa ggcaaaaata tcaggagctt ttttacacac 2040 ctactaaaaa agttattatg tagctgaaac aaaaatgcca gaaggataat attgattcct 2100 cacatcttta acttagtatt ttacctagca tttcaaaacc caaatggcta gaacatgttt 2160 aattaaattt cacaatataa agttctacag ttaattatgt gcatattaaa acaatggcct 2220 ggttcaattt ctttctttcc ttaataaatt taagtttttt ccccccaaaa ttatcagtgc 2280 tctgctttta gtcacgtgta ttttcattac cactcgtaaa aaggtatctt ttttaaatga 2340 attaaatatt gaaacactgt acaccatagt ttacaatatt atgtttccta attaaaataa 2400 gaattgaatg tcaatatgag atattaaaat aagcacagaa aatc 2444 <210> SEQ ID NO 113 <211> LENGTH: 1200 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/CCA90206.1 <309> DATABASE ENTRY DATE: 2001-02-03 <313> RELEVANT RESIDUES: (1)..(1200) <400> SEQUENCE: 113 atggctacct tgcacttcgt tcctcagcac gaggaagaac aagtttactc catctctggg 60 aaggcactca agttaacaac cagtgacgat atcaaaccat acctggaaga attggcagct 120 ttgaaaacct gtaccaaatt agacctttca gggaatacaa tcggtactga agcttcggaa 180 gcattagcta aatgcatcgc tgaaaataca caggtcaggg aatctttggt tgaagtaaat 240 tttgctgact tatacacttc gaggttggtt gacgaagtcg ttgattcgtt gaagttttta 300 ttgcctgttc tgttgaaatg tcctcacttg gagattgtga acctttctga taatgcgttt 360 gggctaagaa caatcgagtt actagaagat tacattgcac atgccgtgaa tatcaaacat 420 ttgatcttaa gtaacaatgg tatgggccct tttgctggtg aaaggattgg taaggcccta 480 tttcatctcg ctcaaaataa gaaagctgct tccaaaccat ttttggaaac ttttatctgt 540 ggtagaaata gattagagaa tggatccgca gtctacttag ctctgggttt gaaaagccac 600 tccgaaggtt tgaaagtcgt aaagctgtac caaaatggta ttaggcctaa aggtgtcgcc 660 acgctaattc attacggttt acagtacttg aaaaacttgg aaatcttgga tcttcaagac 720 aatactttca cgaaacatgc ttctttgatc cttgctaagg ccttgcctac atggaaggat 780 agtttatttg aattgaattt gaacgactgt cttttgaaaa ctgctggttc agatgaagtc 840 tttaaagtat tcaccgaagt taaattcccc aatttgcatg tcttgaaatt cgaatataat 900 gaaatggctc aagaaaccat tgaagtatcc ttcttaccgg ctatggaaaa gggaaattta 960 cctgaattgg aaaagctaga aataaatggt aacagattag atgaagattc tgatgcttta 1020 gatttgctcc aaagcaaatt tgatgattta gaggttgacg attttgaaga ggtcgatagt 1080 gaagatgagg aaggcgagga cgaggaagac gaggacgagg atgaaaaact cgaagaaatt 1140 gaaacggaaa ggcttgaaaa ggaactgcta gaagtacaag tagatgatct tgctgaacgt 1200 <210> SEQ ID NO 114 <211> LENGTH: 1245 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 114 atggcatcag tagaagttga attaggagtt actccagaaa ccacttattc aatttcagga 60 aaacaactaa aatttgattc tgaatcggat attgctccat atatcaagga attgacggaa 120 aaagaaaatg tcaaaaaagt tgatttttca ggaaatacta ttggtattga agcatcaaaa 180 gcattaagtg aagcattatt aaaacataaa gacactatcg ttgaaatcaa cttttctgat 240 ttatacactg gtagattgaa tactgaaatt cctcaatctt tagagtattt gttaccagca 300 ttgtcgaaat tgccaaattt gaaattgatc aacttgagtg acaatgcttt tggattgcaa 360 actattgatc caattgaagc ttacttggcc aaagctgttt ccatcgagca tttgattttg 420 tcaaacaatg gtatgggtcc atttgctggg tcaagaattg gaggatcttt gtttaagtta 480 gctaaggcta agaaagcaga aggaaaggag tctttgaaaa catttatttg tggtagaaac 540 agattggaaa atggttctgt taactattta tctgttgggt taagaaatca caaggatttg 600 gaagtggtta gattgtatca aaatggtatt agacctgctg gtatttctaa attggttgag 660 caaggtttat ctaacaacaa aaaattaaaa gtgcttgatt tgcaagacaa taccatcact 720 accagaggag ctattcacat tgcagaatca ttatctaact ggccactttt ggttgagttg 780 aatcttaacg attccttatt gaagaacaaa ggttctttga aattagtcga agccttccat 840 gctggagatg aaaaaccgca attaattacc ttgaaattac aatataatga gttagaaaca 900 gatagtttaa gagttttggc tgatgcaatt gccagtaaat taccacaatt gaagttcttg 960 gaattgaacg gtaatagatt tgaagaggat tccgaacata tcgataaaat caatggaatc 1020 ttcgaagaaa gaggctatgg cgaaatagat gaattggatg aattagaaga gcttgatagt 1080 gaagaagaag aagatgacga ggatgacgaa ggagaagacg acacattaga ggaagacctt 1140 gatttgacac aattagaaga agaattggct ggagtttctt tggaagacaa agatggtaac 1200 gtggatgaaa ttgccgaaga attatccaaa actcatatta aatag 1245 <210> SEQ ID NO 115 <211> LENGTH: 1788 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/X82260.1 <309> DATABASE ENTRY DATE: 1995-05-11 <313> RELEVANT RESIDUES: (1)..(1788) <400> SEQUENCE: 115 atggcctcgg aagacattgc caagctggca gagacacttg ccaagactca ggtggccggg 60 ggacagctga gtttcaaagg caagagcctc aaactcaaca ctgcagaaga tgctaaagat 120 gtgattaaag agattgaaga ctttgacagc ttggaggctc tgcgtctgga aggcaacaca 180 gtgggcgtgg aagcagccag ggtcatcgcc aaggccttag agaagaagtc ggagttgaag 240 cgctgccact ggagtgacat gttcacggga aggctgcgga ccgagatccc accagccctg 300 atctcactag gggaaggact catcacagct ggggctcagc tggtggagct ggacttaagc 360 gacaacgcat tcgggcccga cggtgtgcaa ggcttcgagg ccctgctcaa gagctcagcc 420 tgcttcaccc tgcaggaact caagctcaac aactgtggca tgggcattgg cggcggcaag 480 atcctggctg cagctctgac cgaatgtcac cggaaatcca gtgcccaagg caagcctctg 540 gccctgaagg tctttgtggc tggcagaaac cgtctggaga atgatggcgc cactgccttg 600 gcagaagctt ttagggtcat cgggaccctg gaggaggtcc acatgccaca gaatgggatc 660 aaccaccctg gcatcactgc cctggcccag gctttcgctg tcaaccccct gctgcgggtc 720 atcaacctga atgacaacac cttcactgag aagggcgccg tggccatggc cgagaccttg 780 aagaccttgc ggcaggtgga ggtgattaat tttggggact gcctggtgcg ctccaagggt 840 gcagttgcca ttgcagatgc catccgcggc ggcctgccca agctaaagga gctgaacttg 900 tcattctgtg aaatcaagag ggatgctgcc ctggctgttg ctgaggccat ggcagacaaa 960 gctgagctgg agaagctgga cctgaatggc aacaccctgg gagaagaagg ctgtgaacag 1020 cttcaggagg tgctggaggg cttcaacatg gccaaggtgc tggcgtccct cagtgatgac 1080 gaggacgagg aggaggagga ggaaggagaa gaggaagaag aggaagcaga agaagaggag 1140 gaggaagatg aggaagagga ggaagaagag gaggaggagg aggaagaaga gcctcagcag 1200 cgagggcagg gagagaagtc agccacgccc tcacggaaga ttctggaccc taacactggg 1260 gagccagctc ccgtgctgtc ctccccacct cctgcagacg tctccacctt cctggctttt 1320 ccctctccag agaagctcct gcgcctaggg cccaagagct ccgtgctgat agcccagcag 1380 actgacacgt ctgaccccga gaaggtggtc tctgccttcc taaaggtgtc atctgtgttc 1440 ttagctgaaa ctgaaatcaa atagaaggac gaagctactg tgaggatggc agtgcaggat 1500 gcagtagatg ccctgatgca gaaggctttc aactcctcgt ccttcaactc caacaccttc 1560 ctcaccaggc tcctcgtgca catgggtctg ctcaagagtg aagacaaggt caaggccatt 1620 gccaacctgt acggccccct gatggcgctg aaccacatgg tgcagcagga ctatttcccc 1680 aaggcccttg cacccctgct gctggcgttc gtgaccaagc ccaacagcgc cctggaatcc 1740 tgctccttcg cccgccacag tctgctgcag acgctgtaca aggtctag 1788 <210> SEQ ID NO 116 <211> LENGTH: 1140 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/AAB67337.1 <309> DATABASE ENTRY DATE: 1997-08-22 <313> RELEVANT RESIDUES: (1)..(1140) <400> SEQUENCE: 116 atgtcctctc aagcattcac ttcagtacat ccgaatgcgg caacatctga tgtgaatgtt 60 accattgaca ctttcgttgc taagttaaaa agaagacaag tgcaaggttc atacgccatc 120 gccttggaaa ctttacaact gttaatgcga tttatctctg cagctcgttg gaaccatgtt 180 aatgacctta ttgaacaaat cagagattta ggtaatagtc tagaaaaagc tcatcctact 240 gctttcagtt gcggtaacgt aattagaaga atactggctg ttttgaggga tgaagtagaa 300 gaagacacta tgagcacaac tgtcacatcc acatccgttg ctgaaccttt gatttcctct 360 atgtttaatt tattacagaa accggagcaa cctcatcaga atagaaaaaa tagttcaggg 420 agctctagta tgaaaaccaa gactgattac cgtcaagtag ccattcaggg tatcaaggat 480 cttatagatg agataaaaaa cattgatgaa ggtattcagc aaattgctat tgatttgatt 540 cacgatcatg agattttatt aactcccaca cctgattcaa aaaccgtatt aaaatttctg 600 attactgctc gcgaacgtag taatagaaca tttacggttt tagttacaga ggggttccct 660 aataacacca agaatgcaca tgagtttgcc aaaaaattag cacagcacaa catagaaacc 720 ctagtagtcc cagactcagc tgtttttgct ttaatgtccc gtgtgggtaa ggttattatc 780 ggcactaaag ccgtttttgt caatgggggg actatctcgt caaattcagg tgtatcatcc 840 gtttgtgaat gcgcccgaga atttagaacc cctgtatttg ctgttgcagg tttgtataag 900 ctttctcctc tatatccgtt cgacgtagag aagtttgtcg aatttggtgg gtcccaacgt 960 atattaccta gaatggatcc aagaaaaaga ttagatacag ttaatcaaat taccgattat 1020 gttccgcctg aaaatattga tatctacatt acaaacgtcg gtgggttcaa tccaagtttt 1080 atatatcgta ttgcgtggga taattacaag caaattgatg tgcatttgga taaaaataag 1140 <210> SEQ ID NO 117 <211> LENGTH: 1098 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 117 atgtcgaaat tgcttactcc tgaaattcta gcgctcatag acccagtggt gtctagtttg 60 aaacgtcatc agcttgtgga tgataaggag atagcattaa caattgccca gttgttgatg 120 aaagtcatat cagcagcaag atggtctaat acatatgatt taattgaatt gataagacaa 180 gttggtgtta tatttaccga agcatatcct agaaaagtca ttccaggaaa tattgtgaga 240 agagtgttag ctttaatacg tgatgaaacc gaaactgaaa ctgagacaga gactgaacaa 300 acagataaca tcccaatgat gagctctatg tttagtttat tggcaacaca taacaaaaat 360 gaaactataa aggaacaaac acaattacaa ctgaagaaac aaacaagcga tatgagagcc 420 ataattatac aagggattag agatttagtt gatgaaattt ccaatgttaa tgatgggatt 480 gaaactatgg cggttgattt gattcatgac gatgaaatat tattaactcc aacccctaat 540 tcggaaacag tgcaacattt tttaatcaaa gcaagattga aaagaaaatt cacagtagtt 600 gttactgaaa actatccaaa cgacatcaag gcagcccaca agtttgtaaa gacactagct 660 gaacacaaca tcgaaacaat tttaattcca gacacaacaa tttatgcagt gatgtcaaga 720 gttgggaaag ttataatagg tactaatgct gtatttgcca atggtggctg tttgtcagat 780 tcaggtgttg ccaatgtagt tgaatgtgcc aaagaacaca gaacacctgt gtttgctgtg 840 gcagggttat tcaaattatc tccattgtat ccatttacaa gaaacgattt gattgaagta 900 ggaaactccg ggaaggtttt gaactacgac gattttgaat tggtacaaaa tgttgatgtt 960 gtgactaatc ctttggaaga ttatatacct cctcaacata tcgacatttt tatgaccaat 1020 attggagggt tttctccttc atttatttat agaattgttt tggataatta taaagctgaa 1080 gacaacaaac ttgaataa 1098 <210> SEQ ID NO 118 <211> LENGTH: 1450 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <220> FEATURE: <221> NAME/KEY: misc_feature <222> LOCATION: (1367)..(1367) <223> OTHER INFORMATION: n is unknown <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/L40395.1 <309> DATABASE ENTRY DATE: 1997-08-22 <313> RELEVANT RESIDUES: (1)..(1450) <400> SEQUENCE: 118 aaaaagggtt cggagttgtc agagaggatc gagagcttcg tggagaccct gacgcggggt 60 ggtgggccgc gcaggtccga ggaaatggtc gggagaccct agggttgctg cgccagatca 120 tcacggacca ccgatggaga aacgcggggg agctgatgga gctgatccgc agagagggca 180 ggaggatgac ggccgctcag ccctccgaga ccaccgtggg caacatggtg cggagagtgc 240 tcaagattat ccgggaggag tatggagact ccatggacgc agcgacggag agtgatcagc 300 aggagtccct ggacaaactg ttgacayccg gaggcctaaa cgaggatttc agcttccatt 360 atgsccaact ccagtccaac atcattgagg cgattaatga gctgctagtg gagctggaag 420 ggacaatgga gaacattgca gcccaggctc tggagcacat tcactccaat gaggtgatca 480 tgaccattgg cttctcccga acagtagagg ccttcctcaa agaggctgcc cgaaagagga 540 aattccatgt cattgtagca gagtgtgctc ctttctgcca gggtcatgaa atggctgtga 600 atttgtccaa agcaggtatt gagacaactg tcatgactga tgctgccatt tttgccgtta 660 tgtcaagagt caacaaggtg atcattggca ccgaagacca tcctggccaa tggggccctg 720 agagctgtga caggaactca cactctggca ctggcagcaa aacaccattc caccccactc 780 atcgtcttgt gcacctatgt tcaaactttc tccacagttc cccaatgaag rrgmcycatw 840 wmataagttt ggtggctcct gaagaagtcc tgccattcac agaaggggam atyctggaga 900 aggtcagcgt gcattgycct gtgtttgact acgytccccc agagctcawt accctcttta 960 gcgtgatctc caacattggt gggaatgcac cttcttacat ctaccgcctg atgagtgaac 1020 tctaccatcc tgatgawcat gttttatgac cgaccacacg tgtcctaagc agattgctta 1080 ggcagataca gawtgaagag gagacttgag tgttgctgct gaagcacatc cttgcaatgt 1140 gggagtgcac aggagtccac cwaaaaaaaa aatccttgat actgttgcct gcctttttag 1200 tcaccccgta acaagggcac acatmcagca ytgtgtcttg cctttcagat cttaacagag 1260 cagcagggct taacttgttg atttkggags ctcttagtga cctggttgcg tctgtgtcag 1320 gaacttaaac tttctggttc agtagtgtgk taaacataac rctgwanacc ttactgggat 1380 acagattttt gctcagaaat ggctatgaca ctttttctag gctctaccaa taaaarccac 1440 ttgaaggttc 1450 <210> SEQ ID NO 119 <211> LENGTH: 720 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/CAA97221.1 <309> DATABASE ENTRY DATE: 1997-08-11 <313> RELEVANT RESIDUES: (1)..(720) <400> SEQUENCE: 119 atgtcaagac tagaaatata ctcgccagaa gggctacgtc tcgatggacg tcgatggaat 60 gaactccgcc gttttgaaag ttccatcaac acacatccgc acgctgcaga cggttcatcc 120 tacatggaac aaggtaacaa caaaattatc actcttgtta aaggtccaaa agagccaaga 180 ttgaaatctc aaatggatac ctcaaaggct ttattgaacg tatcggtaaa cattacaaaa 240 ttctccaaat tcgaaagaag taaatcaagc cacaagaatg aaaggcgtgt tcttgagata 300 caaacctccc tggtgaggat gtttgagaag aatgtcatgc tgaatatcta ccccagaaca 360 gttatcgata tcgagatcca tgtccttgag caagatggcg gtattatggg atctttaatc 420 aacggtatta ccctcgcttt aatagatgcc ggtatatcaa tgttcgatta cataagtggt 480 atatccgtcg ggctgtacga tactacccca ttattagata ccaattcatt agaagaaaat 540 gctatgagta cagtgacact aggtgtggta gggaagtcag aaaaactttc tcttttattg 600 gtggaagaca aaattccgtt agataggtta gagaacgttc ttgccatcgg catcgcaggt 660 gctcataggg taagagattt gatggatgaa gaactgagga aacatgctca gaaaagagtc 720 <210> SEQ ID NO 120 <211> LENGTH: 723 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 120 atggaattat attcacctga gggacttaga atagacggaa gaagatggaa cgaattgcgt 60 agatttgaat gccgtatcaa cactcatcca aactcatcgg atggctcctc atatgtcgaa 120 caaggtaata ccaaagtgat gtgcacagta caaggaccaa tagaaccagc attaagatct 180 caacaacatt cagaacgagc aaatatagaa gtgaatttga atattgctag tttttcaact 240 tttgaaagga aaaaacgaag tagaaatgaa agaagattag ttgaacttaa aactacttta 300 gaaaaaacat ttgaagaaag tgttatgata aatttatatc caagaacaaa tattgttata 360 aatgttcaag tattatgcca ggatggtggg atgttagctg cagttatcaa ctctattaca 420 ttagcactca ttgacgctgg tatatcaatg tatgattatg tgagtggtgt atcttgtgga 480 ttatatgatc aaacaccatt attagatgta aataacttag aagaacacga tatgagttgt 540 ttaacagttg gtgttattgg taaaagtgag aaattggcat taatgttgtt agaagataaa 600 atgccattgg atagattgga atcagtattg tcaattggta ttgctggaag tcataaaata 660 agagaattaa tggatcaaga agtgaggaag catggaatta ttagggcttc taaaatgcaa 720 taa 723 <210> SEQ ID NO 121 <211> LENGTH: 840 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/AK000598.1 <309> DATABASE ENTRY DATE: 2000-02-22 <313> RELEVANT RESIDUES: (1)..(840) <400> SEQUENCE: 121 agagagcgga cctggcggcc gggcagcatg gcggggctgg agctcttgtc ggaccagggc 60 taccgggtgg acgggcggcg cgccggggag ctgcgcaaga tccaggcgcg gatgggcgtg 120 ttcgcgcagg ctgacggctc ggcctacatt gagcagggca acaccaaggc actggctgtg 180 gtctacggcc cgcacgagat ccggggctcc cgggctcgag ccctgccgga cagggcccta 240 gtgaactgtc aatatagttc agcgaccttc agcacaggtg agcgcaagcg acggccacat 300 ggggaccgta agtcctgtga gatgggcctg cagctccgcc agactttcga agcagccatc 360 ctcacacagc tgcacccacg ctcccagatt gatatctatg tgcaggtgct acaggcagat 420 ggtgggacct atgcagcttg tgtgaatgca gccacgctgg cagtgctgga tgccgggata 480 cccatgagag actttgtgtg tgcgtgctca gctggcttcg tggacggcac agccctggcg 540 gacctcagcc atgtggagga agcagctggt ggcccccagc tggccctggc cctgctgcca 600 gcctcaggac agattgcgct gcttgagatg gatgcccggc tgcacgagga ccacctggag 660 cgggtgttgg aggctgctgc ccaggctgcc cgagatgtgc acaccctctt agatcgagtg 720 gtccggcagc atgtgcgtga ggcctctatc ttgctggggg actgaccacc cagccaccca 780 tgtccagaat aaaaccctcc tctgcccaca caaaaaaaaa aaaaaaaaaa aaaaaaaaaa 840 <210> SEQ ID NO 122 <211> LENGTH: 2340 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/A46417 <309> DATABASE ENTRY DATE: 1998-02-06 <313> RELEVANT RESIDUES: (1)..(2340) <400> SEQUENCE: 122 atgtcccgtt tcttttcgtc taattacgaa tacgatgtag ccagttcttc atccgaagaa 60 gatcttttat cttcgtctga agaagatttg ttaagctctt cctcctctga gtctgaattg 120 gaccaagaat ctgacgactc ctttttcaat gaaagtgaaa gtgaaagtga agctgatgta 180 gactctgatg attctgatgc aaagccttat ggtcctgact ggttcaagaa atctgagttc 240 agaaaacaag gtggaggttc aaataaattt ttgaaaagct ctaactatga ttccagtgat 300 gaagaatccg atgaagaaga tggcaagaag gtagtcaagt ctgccaaaga aaaactattg 360 gatgaaatgc aagacgttta taataagatc tctcaagctg agaactctga tgactggttg 420 actatttcta atgagtttga tttgatctcg cgtctcttag ttagggctca acaacaaaac 480 tgggggactc caaatatttt catcaaggtt gttgcccaag tggaggacgc tgtgaataat 540 acacaacaag ctgatttgaa gaataaagct gttgcaagag cttataacac tacaaagcaa 600 agagtcaaga aagtttctag agaaaatgaa gactcaatgg ctaaattcag aaatgatcct 660 gaatcatttg ataaggaacc aaccgcagat ttggatattt ctgctaatgg attcacaatt 720 tcttcgtctc aaggcaatga ccaagcggta caagaagatt tcttcactag attacaaaca 780 ataattgact caagaggtaa gaagactgtc aatcaacaat ccttgatttc tactttggag 840 gagttattaa ctgtagctga aaaaccatat gaattcataa tggcttattt gactttgatt 900 ccatcaagat tcgatgcctc agctaaccta tcttaccaac caattgatca atggaaatct 960 tcattcaacg atattagtaa attattgtct attttagacc agacaattga cacctaccaa 1020 gttaatgaat ttgctgatcc aatcgatttc attgaagatg aacctaaaga agattctgat 1080 ggtgtcaaga ggattctggg ttccattttc tcatttgttg aaagattaga tgacgaattc 1140 atgaaatccc tgttaaacat cgatcctcat tccagtgatt atttgatccg tttaagggat 1200 gaacaatcaa tctataattt gatcctaaga actcaattgt actttgaagc gactttgaaa 1260 gatgaacacg acctagaaag agcattgaca cgtccattcg tcaagagatt ggatcatatc 1320 tactataaat ccgaaaattt gataaaaatt atggaaactg ctgcttggaa tatcatacct 1380 gctcaattca aatctaaatt tacttcaaaa gaccagctcg attctgctga ttatgtcgac 1440 aatttaatag acggattatc gacaatctta tccaagcaaa acaacattgc tgttcaaaaa 1500 cgtgctattt tatacaacat ttactacact gcattaaaca aagatttcca aactgctaaa 1560 gatatgttac taacttccca agttcaaaca aatatcaacc aattcgattc atccctacaa 1620 attttattca acagggttgt tgttcaattg ggtctatccg cctttaaatt atgtttgatt 1680 gaagaatgtc atcaaatttt gaatgatctt ctgtcaagtt ctcacttaag agaaattttg 1740 ggccaacaat ccctacacag aatatctctc aattctagta acaatgcttc agctgatgag 1800 cgtgctagac aatgtttgcc atatcaccaa cacatcaatc tcgatttaat cgatgtcgtc 1860 ttcttaacat gttccttatt gatcgaaatt ccaagaatga ctgccttcta ttccggtatt 1920 aaggtcaaga gaattcctta ctctccaaaa tccattcgtc gttccttaga acattacgac 1980 aagttaagtt tccaaggtcc accagaaact ttaagagatt atgtcttgtt tgctgccaaa 2040 tcaatgcaaa aaggtaactg gagagactct gttaaatact taagagaaat aaaatcttgg 2100 gctttattac caaacatgga aacggtgttg aatagtttaa cggaaagagt acaagttgaa 2160 tctttgaaga cttatttctt ttctttcaag aggttctatt caagtttttc tgttgctaaa 2220 ctagccgaat tatttgatct tccagaaaat aaggtggttg aagttttgca atctgttatc 2280 gcagaattgg aaatcccagc caaattaaac gacgagaaga ccatctttgt tgtcgaaaag 2340 <210> SEQ ID NO 123 <211> LENGTH: 2099 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 123 atgtctcgtt tttttgtttc aggatacact tctgactctt cttctgaaga ggaggattta 60 ttgagtactt ctgaagaaga gttattatct tcttctgatg aaggagaaga caacgaatca 120 gatagttcat tttttggtga agatgatgat gaatcagaag aatctagttc tgatgatgaa 180 gatggtcgac catctggtcc agcatatttt ttaaagaaat catttttaaa aggagctgga 240 ggagatgatt ctgacagtga tagtgatgat gaaggtcgta aagttgttaa atcagctaaa 300 gataaattat tagatgatat gaaatcttca attgaaatta taaattccaa caaatataat 360 aacaattgga gtatagtttt aggtgaattt gataagtttg gtagattttt gattagatgt 420 aatcaaacca atttgggtac accaaaattt tatattaaat tgttgactag tttagataac 480 tccataactg aaactagtaa taatgaaaga gatgataaaa cattaaaagc tgatgaagcc 540 agagctttca atactttgag acaaagaatt aaaaaacaaa taagagaatt ccaagtttat 600 tatgatttgt ataaggaaaa tccagaagaa tttgatgaaa atgaagatga accattagaa 660 tctgttcaag ctggtcttaa cgataatgtt aaaaatgaag ctgataattc taatgttggt 720 gctcttgcgt caaacagagt attgagtcct attttccata ctttgaaaac tatttccgaa 780 agtcgtggta aaaagaatat tgataaattg gaacaaattg ctactttgga aaaattatta 840 gaagcaaatg tttctaaaag ttcaccattt gaattgattt ctatttatca gatgttatta 900 tcagttagat ttgatgcttc atctaatcaa gcttttatgc ctttggaaca atggcaaaag 960 aatgaacacg atttaggtaa attattggat ttgttggaag ctaatgttga tacttatcaa 1020 gtttctgaat tgggttcaac tactgatgat attgatattg aaccagttgc taatgcccaa 1080 ggtgttaaag ttattttcgg atcaatcact tcttctattg atagattgga cgatgaattg 1140 accaaatctt tacaacatac tgacccacat tctattgaat atgttgaaag attgaaggat 1200 gaaagtacta tttacaattt gattgttaga ggtcaagcat atgttgaatc cataactcca 1260 gaagatgtca agtataattc tgaacaattg gcaagaattg ttttgagaag attggaacac 1320 atttattata aaccaaaaca attgattaaa gctaatgaag aagaagcttg gcgtaatatt 1380 gaatacaatt catctattgt cagtaaaggt tcttcagttg atgaagttat tgatcaattg 1440 acggaatttt tacaaaagca acaaaaaaac aaaacttatg ggaaacatgc tatactattc 1500 tccatttatt attatgctgt caatagtcaa tatgaaaagg ctaaagaatt atttttgaga 1560 tctcaatttt atagtaacat caattctgct gaatcttctt tacaagttca atataatcgt 1620 gctttagttc aattaggttt aagtgctttt agagcaggta gtattgaaga atctcataaa 1680 attttgaatg aaattgtcaa ttctcaaaga tctaaagaat tattgggtca aggtttcaat 1740 tctaaattcc ccaatcaagc tactgttttg gaaagacaaa aattattacc attccatcaa 1800 catattaatt tggaattatt ggaatgtgta tttatgactt gttctttatt aattgaaatt 1860 ccaactttgg ctgctattgc taataatcat aaggattcaa aacgtaaaaa tgcttcattg 1920 aaatctttca aaagtaaatt ggatttccat gatagacaat ttttcactgg tccaccagaa 1980 agtattaaag atcatattgt ggtgatgaaa ttactaaatt ggaagaagca atggtaaaat 2040 tgaacaaaga atataaaatc gctaaagaac gtcttaaccc accatcaaat cgtcgttga 2099 <210> SEQ ID NO 124 <211> LENGTH: 2898 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/U46025.1 <309> DATABASE ENTRY DATE: 1999-01-08 <313> RELEVANT RESIDUES: (1)..(2898) <400> SEQUENCE: 124 tgactcgcgg gctcagctgg tccggccgta gcacctccgc gccgtcgcca tgtcgcggtt 60 tttcaccacc ggttcggaca gcgagtccga gtcgtccttg tccggggagg agctcgtcac 120 caaacctgtc ggaggcaact atggcaaaca gccattgttg ctgagcgagg atgaagaaga 180 taccaagaga gttgtccgca gtgccaagga caagaggttt gaggagctga ccaaccttat 240 ccggaccatc cgtaatgcca tgaagattcg tgatgtcacc aagtgcctgg aagagtttga 300 gctcctggga aaagcatatg ggaaggccaa aagcattgtg gacaaagaag gtgtcccccg 360 gttctatatc cgcatcctgg ctgacctaga ggactatctt aatgagcttt gggaagataa 420 ggaagggaag aagaagatga acaagaacaa tgccaaggct ctgagcacct tgcgtcagaa 480 gatccgaaaa tacaaccgtg atttcgagtc ccatatcaca agctacaagc agaaccccga 540 gcagtctgcg gatgaagatg ctgagaaaaa tgaggaggat tcagaaggct cttcagatga 600 ggatgaggat gaggacggag tcagtgctgc aactttcttg aagaagaaat cagaagctcc 660 ttctggggag agtcgcaagt tcctcaaaaa gatggatgat gaagatgagg actcagaaga 720 ttccgaagat gatgaagact gggacacagg ttccacatct tccgattccg actcagagga 780 ggaagaaggg aaacaaaccg cgctggcctc aagatttctt aaaaaggcac ccaccacaga 840 tgaggacaag aaggcagccg agaagaaacg ggaggacaaa gctaagaaga agcacgacag 900 gaaatccaag cgcctggatg aggaggagga ggacaatgaa ggcggggagt gggaaagggt 960 ccggggcgga gtgccgttgg ttaaggagaa gccaaaaatg tttgccaagg gaactgagat 1020 cacccatgct gttgttatca agaaactgaa tgagatccta caggcacgag gcaagaaggg 1080 aactgatcgt gctgcccaga ttgagctgct gcaactgctg gttcagattg cagcggaaaa 1140 caacctggga gagggcgtca ttgtcaagat caagttcaat atcatcgcct ctctctatga 1200 ctacaacccc aacctggcaa cctacatgaa gccagagatg tgggggaagt gcctggactg 1260 catcaatgag ctgatggata tcctgtttgc aaatcccaac atttttgttg gagagaatat 1320 tctggaagag agtgagaacc tgcacaacgc tgaccagcca ctgcgtgtcc gtggctgcat 1380 cctaactctg gtggaacgaa tggatgaaga atttaccaaa ataatgcaaa atactgaccc 1440 tcactcccaa gagtacgtgg agcacttgaa ggatgaggcc caggtgtgtg ccatcatcga 1500 gcgtgtgcag cgctacctgg aggagaaggg cactaccgag gaggtctgcc gcatctacct 1560 gctgcgcatc ctgcacacct actacaagtt tgattacaag gcccatcagc gacagctgac 1620 cccgcctgag ggctcctcaa agtctgagca agaccaggca gaaaatgagg gcgaggactc 1680 ggctgtgttg atggagagac tgtgcaagta catctacgcc aaggaccgca cagaccggat 1740 ccgcacatgt gccatcctct gccacatcta ccaccatgct ctgcactcgc gctggtacca 1800 ggcccgcgac ctcatgctca tgagccactt gcaggacaac attcagcatg cagacccgcc 1860 agtgcagatc ctttacaacc gcaccatggt gcagctgggc atctgtgcct tccgccaagg 1920 cctgaccaag gacgcacaca acgccctgct ggacatccag tcgagtggcc gagccaagga 1980 gcttctgggc cagggcctgc tgctgcgcag cctgcaggag cgcaaccagg agcaggagaa 2040 ggtggagcgg cgccgtcagg tccccttcca cctgcacatc aacctggagc tgctggagtg 2100 tgtctacctg gtgtctgcca tgctcctgga gatcccctac atggccgccc atgagagcga 2160 tgcccgccga cgcatgatca gcaagcagtt ccaccaccag ctgcgcgtgg gcgagcgaca 2220 gcccctgctg ggtccccctg agtccatgcg ggaacatgtg gtcgctgcct ccaaggccat 2280 gaagatgggt gactggaaga cctgtcacag ttttatcatc aatgagaaga tgaatgggaa 2340 agtgtgggac cttttccccg aggctgacaa agtccgcacc atgctggtta ggaagatcca 2400 ggaagagtca ctgaggacct acctcttcac ctacagcagt gtctatgact ccatcagcat 2460 ggagacgctg tcagacatgt ttgagctgga tctgcccact gtgcactcca tcatcagcaa 2520 aatgatcatt aatgaggagc tgatggcctc cctggaccag ccaacacaga cagtggtgat 2580 gcaccgcact gagcccactg cccagcagaa cctggctctg cagctggccg agaagctggg 2640 cagcctggtg gagaacaacg aacgggtgtt tgaccacaag cagggcacct acgggggcta 2700 cttccgagac cagaaggacg gctaccgcaa aaacgagggc tacatgcgcc gcggtggcta 2760 ccgccagcag cagtctcaga cggcctactg agctctccac tctgtttccc gcctgggcca 2820 tccaaccttg aagtcctaaa ccacacctca gtcactaaag gtctgtttaa agttgttctg 2880 gttgattgct tgttgcca 2898 <210> SEQ ID NO 125 <211> LENGTH: 1020 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/AAC03225.1 <309> DATABASE ENTRY DATE: 2000-10-10 <313> RELEVANT RESIDUES: (1)..(1020) <400> SEQUENCE: 125 atgtctgaac ttaatgcatt attaaaagat atcaacggct cgctcactgc gacatcagaa 60 tccttggaga ggttgtctgg gatttatagt aattctgcga ccgatgagat tcctgaaagt 120 aaccaactac atgagcatct attttacgac gctaagaagc ctgctgagaa agtatcgctg 180 ctatccttaa aaaatgggag catgctaggg tacataaatt ctctattgat gcttataggc 240 aataggctag acgacgagtg caaagatcct tctgctatgg atgcacgtga acgctctatt 300 caacaccgtg tggtattaga gcgtggtgtt aaaccactag aaaaaaagtt ggcttaccaa 360 ttggacaagc tgactagagc atatgtgaaa atggaaaagg aatataaaga cgctgagaag 420 cgtgcactgg aaaaatctac cttagtgaat catagcggca acgacgatag cgaagatgat 480 gagtctagtg aggatgaaat agcatacagg ccaaatacct ctggaattat caacacaaat 540 aaaaaatcat cagcatacag ggtggaggaa acggctaagc aagaaaacgg ggaagaaaac 600 gatgacaatg agactggcgt gtataaacca ccaaagatta cggctgttct accaccgcaa 660 caaacgcatt ttgaagatag attcgatgcc agagaacaca aagatcgtag taacaaatcg 720 cgtatgcaag ccatggaaga atatattaga gagtcatcgg accaaccgga ctggagtgca 780 tctattggtg ctgacattgt gaaccatgga agaggcggta tcaaatcttt gagagacaca 840 gagaaggaac gtagagtcac ttcattcgaa gaagataatt ttaccagatt gaatattaca 900 aataaagctg aaaaaaggaa gcaaaagcaa cgagaaagaa atgcaaggat gaacgttatc 960 ggtggtgaag attttggtat attcagctca aagaggaagc tggaagatag cacttcgaga 1020 <210> SEQ ID NO 126 <211> LENGTH: 1086 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 126 atgtcaaagg tagacactgt attaaaggaa atcatctcgt ctaccaagtc aactgaagct 60 tcagtgaaag agttgatagc ttttgtcaag gactcgtctt cccaacatcc agaattggtg 120 cggaacttgt tagcaaaatc aaacctgctg ttagaagggg tatcgttgtt ggggttgaaa 180 aacgaatcgt tggtgtccta tatcaacaat atagtgcttg ttgttttgtc tcatctagag 240 cgtctagaaa gcgatctgga gacgggatcc agcgctgtcg aacgatcgat aattcaaagg 300 gtgacattgg aaaagggcgt taaacctcta gaaaagaaac tcagttatca gttggataaa 360 atgatcaggg catatggacg gatggaacaa gacgaaatca aagctgaaca gaagttaaac 420 gatagaggaa gtggggagaa cgatgagaac gatgagaacg attctgagga agattctgaa 480 gaagattctg aagacgactc tgaggacgac gaattggctt atagaccaga tgcatcatcg 540 tttgctaaat tgacatcggc caaaaccaaa ctgaaaccaa catcatcagc agtctctaca 600 tcgaatgaaa agtatagacc accaaagata tcagcaatgg cacctccaac tgcagtaaag 660 agccacgacc ttgatgccaa caccacgtcg tcaaagaacc gtaaattaca gagcatggaa 720 gagtacttgc aagagcaaag tgatatgcca atggtggagg catcggtggg gtctacaatt 780 gtggagcatg gaagaggtgg tgttaaaaca cagcacgatc gtaagaaaga acgagagata 840 caaacgtatg aagaggataa ttttgtcaga ctaccaacca gtcaaacaaa gaaaagtttc 900 aaggaaaaac aacgtgatat ccgtaatcaa tttgctggtg aagactggtc gatgtttaat 960 aataacaagg atgtgacccg tcaaggcaca tcgcgaaaga gaaaggcaac caccgtttgg 1020 gacaaagtca agaaaaagaa gaatacttag atggtaagta gacgctgaca ttttgctgca 1080 gtatag 1086 <210> SEQ ID NO 127 <211> LENGTH: 1134 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/AL050003 <309> DATABASE ENTRY DATE: 2000-02-18 <313> RELEVANT RESIDUES: (1)..(1134) <400> SEQUENCE: 127 gggggctttg cgaagatggc ggcgctgggg gtgctggagt ccgacctgcc aagtgccgtg 60 acacttctga aaaatctcca ggagcaagtg atggctgtaa ctgcacaagt gaaatcactg 120 acacaaaaag ttcaagctgg tgcctatcct acagaaaagg gtctcagctt cttggaagtg 180 aaagaccagc tgctgctcat gtaccttatg gatttgaccc acctcattct ggacaaagcc 240 tcaggaggat ctcttcaggg acatgatgca gttttgagac tggtggagat tcgcacggtt 300 ttggaaaagc ttcgtccctt ggaccaaaag ctgaagtatc aaattgacaa gctgatcaag 360 actgcagtga caggcagcct tagtgagaat gacccacttc gttttaagcc tcatcccagc 420 aatatgatga gcaagttgag ctctgaggat gaggaggaag atgaagcaga agatgaccag 480 tctgaggctt cagggaagaa atctgtgaag ggagtgtcta agaaatatgt tcctccacgc 540 ttggttccag tacattatga tgaaacagaa gctgagcggg agaagaagcg tctagaacga 600 gccaagagac gggcattgag cagctctgtc attcgtgaac ttaaggagca gtactcagat 660 gctccagagg aaatccgtga tgctcggcat ccccatgtta cccgccagag tcaggaggac 720 caacacagga ttaactatga ggagagcatg atggtgcgtt tgagcgtcag taagcgagag 780 aaaggacggc gaaaacgagc aaatgtcatg agctcacaac ttcattccct tacacacttc 840 agtgacatca gtgctttgac agggggaact gttcatcttg atgaggatca gaatcctatt 900 aagaagcgga agaagatacc tcagaaaggt cggaagaaaa aaggccagtg aactgctggg 960 acttaggtga tcaggtgcaa ggtggggagt acaaattgag tctctttgga tttgccattc 1020 tgggtctcac caagccctgt agtatctctt ccatactggg caataatctc cttaggtggg 1080 cgtggggcca agaagactcg ttctgcctgg gatagagctc aaaggagact gtag 1134 <210> SEQ ID NO 128 <211> LENGTH: 666 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/CAA95901.1 <309> DATABASE ENTRY DATE: 1997-08-11 <313> RELEVANT RESIDUES: (1)..(666) <400> SEQUENCE: 128 atgagcgcta ccgaatcttc atctatattc acattgagtc acaactcaaa cctacaagat 60 atcttggccg ccaatgccaa atgggcctcc cagatgaaca acatacagcc aactttgttc 120 ccagatcaca atgcgaaggg ccagtcccct cacactcttt tcatcggctg ctccgattcg 180 cgttacaacg aaaactgttt aggtgtcttg cccggcgaag tgttcacttg gaaaaatgtt 240 gctaacatat gtcactcaga ggatttaact ttgaaggcca ctttagagtt tgccattatt 300 tgtctaaaag ttaacaaagt tattatttgt ggccacactg attgtggtgg tataaagaca 360 tgtttaacta accaaaggga agccttacca aaagttaact gttctcatct gtacaagtac 420 ttagacgata ttgacaccat gtaccatgaa gagtcacaaa atttgatcca tttgaaaacg 480 caacgtgaaa aatctcatta cctgtcgcac tgtaacgtca aaaggcagtt taataggatt 540 attgaaaacc ctactgtgca aactgctgta caaaatggag aattacaggt atacggtctg 600 ctttacaacg tagaggacgg tctactgcaa acagttagca cttacacaaa agttacccca 660 aaatag 666 <210> SEQ ID NO 129 <211> LENGTH: 846 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 129 atgggtagag aaaatatttt gaaatatcaa ttggaacatg atcatgaatc tgatcttgtt 60 actgaaaaag atcaatcatt attacttgat aataataaca acctaaacgg gatgaataat 120 accattaaaa ctcatccggt acgtgttagt tcaggaaatc ataataattt tcctttcact 180 ttatcttcag aatctacatt acaagatttt ttaaataata ataaattttt tgttgattcc 240 ataaaacata atcatggtaa tcaaatattt gatttgaatg gtcaaggtca atctcctcat 300 acattatgga tagggtgtag tgattcaaga gcaggtgatc aatgtttagc tacattacca 360 ggagaaatat ttgttcatag aaacattgct aatatagtca atgccaatga tataagtagt 420 caaggggtta tacaatttgc tattgatgta ttaaaagtga aaaaaatcat tgtttgtggt 480 catactgatt gtggtggtat ttgggcatca ttatcaaaga aaaaaattgg tggtgtttta 540 gatttatggt taaatccagt tagacatatt cgtgctgcta atttaaaatt attagaagaa 600 tataatcaag atcctaaatt aaaggccaaa aaattggctg aattaaatgt catttcttct 660 gtaacagcat tgaaaagaca tcctagtgct agtgttgcat taaagaagaa tgaaattgaa 720 gtttggggga tgttatatga tgtggcaact ggttatttat ctcaagtaga gattcctcaa 780 gatgaatttg aggatttatt ccatgttcat gatgaacatg atgaagaaga atataaccct 840 cattga 846 <210> SEQ ID NO 130 <211> LENGTH: 840 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/BAA09266.1 <309> DATABASE ENTRY DATE: 2000-04-14 <313> RELEVANT RESIDUES: (1)..(840) <400> SEQUENCE: 130 atgaaagcta ggaaatcgca gagaaaagcg ggcagtaaac caaatcttat ccagtctaaa 60 ttgcaagtta ataatggttc gaaatcgaat aaaatagtca agtgtgataa atgtgagatg 120 tcatattcct cgacatcaat agaagatcgc gccatccacg agaaatacca cactttacag 180 ctgcatggac gtaaatggtc gccgaattgg ggttctatag tatacacaga gcgaaaccat 240 tcaaggacgg tgcatctatc aagatcgaca gggacaataa cgccattgaa ctcctcacct 300 ttgaaaaaaa gtagtccgtc tattacccat caggaggaga agattgtata tgtgagacca 360 gataagtcga atggtgaagt ccgagccatg acggagataa tgacactagt gaataacgag 420 ctgaatgcgc cacacgatga gaatgtcatt tggaacagta ccacagaaga aaaaggcaaa 480 gcgtttgtat acataagaaa tgacagggcg gtcggaataa taattataga gaacctttat 540 gggggcaatg gtaaaacatc tagtcgtgga cgttggatgg tttatgattc tagaagattg 600 gtacagaatg tgtaccccga ttttaagatt ggcatatcga gaatttgggt gtgcaggaca 660 gcaaggaagt tgggtatcgc aaccaaattg attgacgttg caagagaaaa tattgtttac 720 ggtgaagtta ttcctaggta ccaggtagca tggtcgcaac ccacagacag cggtggaaaa 780 ctggctagca aatacaacgg cattatgcat aaatcaggca agttactatt gccggtatac 840 <210> SEQ ID NO 131 <211> LENGTH: 843 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 131 atgggctcca ttaattctca aaaacctcaa aaaatccaat caattcttgc attaccatct 60 aatttcaaaa aaattacttg ttcaacatgt gatatgacat ataatcccca tatatctcaa 120 gataaattac tacataacaa ataccacaca aatttcatca atggaatacc ctggaattat 180 aaaactgata atgatgtttt aataattgag aattttacat tagttgaaac cccgaaattg 240 aattccacgg ggaaatcatt aaagctgaca aaaacgcgtc agacatttaa aggttctata 300 atttgtataa ataaatccaa caaacgacat atacaaaaag tggaactact attaaacatg 360 gtgaatcaag agttgaatgc tagtcaagat tcaggacaat ggaagaaacc tgaatttgat 420 agaagtaaag catttgtgat aataatagac agtaaggcca ttggattatg cacaacagat 480 acaattcaac ctgatcaagg aaggtggatg atacataaaa cacaatctat agtacctaat 540 cagattaata aaaatgttgt cattggaatt tcaagaatat ggataagtcg gaaatggaga 600 caatatggat taggtaaaaa acttttaaat gttgttttga aaaattctat ttacagtgtg 660 caattattga agaatcaagt tgcctttagt caaccaagtt ttagtggtgg aatgttggca 720 aaatcattca atggggtgaa acataaaagt ggtgaaatgt tgttacccgt atatattgaa 780 tgatcctttc aggttttcgg aggcggcggt gattatgggt gtacatattt gtatattttt 840 tgt 843 <210> SEQ ID NO 132 <211> LENGTH: 1800 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/CAA85033.1 <309> DATABASE ENTRY DATE: 1998-03-16 <313> RELEVANT RESIDUES: (1)..(1800) <400> SEQUENCE: 132 atgctaaatg gggaagactt tgtagagcat aatgatatcc tatcgtctcc ggcaaaaagc 60 aggaatgtaa ccccaaaaag ggttgaccca catggagaaa gacaactgag aagaattcat 120 tcatcaaaga agaatttgtt ggaaagaatc tcgcttgtag gcaacgaaag gaaaaataca 180 tctccagatc cggcactcaa acctaaaacg ccaagtaaag ctccccgtaa acgtggaaga 240 ccaagaaaga tacaggaaga attaactgat aggatcaaga aggatgagaa agatacaatt 300 tcctctaaga aaaagaggaa attggacaaa gatacatcag gtaatgtcaa tgaggaaagc 360 aagacttcta acaacaagca ggtgatggaa aagacgggga taaaagagaa aagagaacgc 420 gaaaaaatac aggtagcgac cacaacatat gaagataatg tgactccaca aactgatgat 480 aattttgtat caaattcacc cgagccacca gaacctgcaa caccatctaa gaagtcttta 540 accactaatc atgattttac ttcgccccta aagcaaatta taatgaataa tttaaaagaa 600 tataaagact caacctcccc aggtaaatta accttgagta gaaattttac tccaacccct 660 gtaccgaaaa ataaaaagct ctaccaaact tcggaaacca agtcagcaag ctcgtttttg 720 gatacttttg aaggatattt cgaccaaaga aaaattgtca gaactaatgc gaagtcaagg 780 cacaccatgt caatggcacc tgacgttacc agagaagagt tttccctagt atcaaacttt 840 ttcaacgaaa attttcaaaa acgtcccagg caaaagttat ttgaaattca gaaaaaaatg 900 tttccccagt attggtttga attgactcaa ggattctcct tattatttta tggtgtaggt 960 tcgaaacgta attttttgga agagtttgcc attgactact tgtctccgaa aatcgcgtac 1020 tcgcaactgg cttatgagaa tgaattacaa caaaacaaac ctgtaaattc catcccatgc 1080 cttattttaa atggttacaa ccctagctgt aactatcgtg acgtcttcaa agagattacc 1140 gatcttttgg tccccgctga gttgacaaga agcgaaacta agtactgggg caatcatgtg 1200 attttgcaga tccaaaagat gattgatttc tacaaaaatc aacctttaga tatcaaatta 1260 atacttgtag tgcataatct ggatggtcct agcataagga aaaacacttt tcagacgatg 1320 ctaagcttcc tctccgtcat cagacaaatc gccatagtcg cctctacaga ccacatttac 1380 gctccgctcc tctgggacaa catgaaggcc caaaactaca actttgtctt tcatgatatt 1440 tcgaattttg aaccgtcgac agtcgagtct acgttccaag atgtgatgaa gatgggtaaa 1500 agcgatacca gcagtggtgc tgaaggtgcg aaatacgtct tacaatcact tactgtgaac 1560 tccaagaaga tgtataagtt gcttattgaa acacaaatgc agaatatggg gaatctatcc 1620 gctaacacag gtcctaagcg tggtactcaa agaactggag tagaacttaa acttttcaac 1680 catctctgtg ccgctgattt tattgcttct aatgagatag ctctaaggtc gatgcttaga 1740 gaattcatag aacataaaat ggccaacata actaagaaca attctggaat ggaaattatt 1800 <210> SEQ ID NO 133 <211> LENGTH: 2130 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 133 atgtcacact caaatgctct accaaatagt ccattccggt cacctaaaaa acaacgtatg 60 gaggtcatag gaccactcaa tgcgtctcgt ttttcctttt cgccggtaaa gacacctcct 120 catgggagag ctggtctatc atctccagag aaaagattag tcaaagacct tgacaagtcg 180 gcgagaaaaa gagccaacaa tagcttatat aaccgattaa tggatgagta tctggacaca 240 gatgattatt tggatgaaca agataggata ttggccgaca gaattatcaa acagtcgagg 300 ggagaacccg acgaagtcaa ttatggcagc gacgtggaat tggaaattga tctaactcag 360 cagagacgaa cccgaagaag agaaaagaaa gttgtttact cgagcgatag tagcaacgaa 420 tatgaggata caggaatgcc agaagaatct tcaagcgagg aagaagaggc agatgatgat 480 gatggcaatg tggagtttgt ttatggacca cccaaagaaa gaaaaacgtc gttatcaagc 540 tcaccaccca cagtcaagcc tactgtgcgc cgaaccaagc gaggtagacc aagcaagagt 600 gagcttgttc tgggtcaaat caaaagtata ttccatcaag atgacgtgtt gttcagtaca 660 gatagaaaaa cgttcacacc gactaaacca accgcagcga aaaaaccagt cagcaattat 720 ttgacatcta tttttgatca aaatttcgat agaagcaagg tgccaagtct aagtggaatt 780 cccaaatcaa ccaacacgca tgaagagaag aaaacgtttg tgccgcttcc tattcccacc 840 ctcgatgctg acggaaatat cactgacaag gagtacatct ccaaatactt tgatggagtt 900 gaccctgcaa agttcaaaga aggcaggttt gtggacgaaa aagtatttta cttagaaggg 960 ccagaaggat actttgaaca gcaaactacc agagttaaac aaagtggcaa ctctttaaca 1020 gcattggcac cccagattga gtacaaagat tttgccaggt tagtaaagtt gggcgacaac 1080 ctcagtttcc aacgcaaacg ccaccttttc gaattgcaca agtatatcta tcaccagtgg 1140 tgttttgaaa tgtcacaagg gttcaatttg aatttctacg gagtcggatc caaaatcgat 1200 ctactccgag attttgccac aaactatttt ggcatctggt gggaaaatgt ggtacacgcc 1260 gatttgccaa aggttttggt ggttaacggt tttaacccta gcatcaatat caaaaaacta 1320 attctcgaaa tcgcttccat ccttttgcca aacgaactgt acccaaaaca tatagctgga 1380 acggttccct ttgtggttga ttatctaaac aaccatagac tgccctgtgg aagtatcggt 1440 ttccataaac ccaaaatctt gttgattatt cacaatcttg atggggaagt ttttagagta 1500 gacaagacac agacgctttt gtcgcaatta atgacactac cagaagtatg ggccatgtca 1560 tctaccgacc acatcaatgc atcattgtta tgggacctgt ccaaagttaa aaacttgaat 1620 ttcatctggc ataatctcac aacatatgcc acttaccaac gagaaacatc tttccgagac 1680 gtgataagtt taggcaaatc caaaaaattt gtgggtggcc ttggtgccaa gtatgtcttg 1740 cgctcgctta ccgacaatca ccgaaacctc taccgcgagc tattgattgc acaattggat 1800 aaaatggaga aagctgtccc atctgcttct ggaagagtgg gtttgaaagg taatgccaag 1860 gttgctgttg acctaaaaag cctatacaat acatgtttgg acgagttcat tacttccaac 1920 gagatgaact ttagaacatt cttaaaagag tatgttgagc ataaaatgtg tcagctagta 1980 aaagatcctt caggagttga gaaggtattc attccgttca catacgaaga gatacaaaac 2040 atatataagc aagaatttga tgtatagtgg gtaccctaca cgtatgcgga acttgaaaaa 2100 cttctgaaaa ccgttttaaa tactctataa 2130 <210> SEQ ID NO 134 <211> LENGTH: 2640 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/GI:4433811 <309> DATABASE ENTRY DATE: 1999-03-18 <313> RELEVANT RESIDUES: (1)..(2640) <400> SEQUENCE: 134 ggcgcgaatt actggaaatt ggcttttccc gttggggccg aaggtacctt ccctgcggcg 60 gcgactcagc ggggtgtcgt tcggccggcg tgacgcagcc ggatcggcgc cagacggaaa 120 cctagcggtg actgtatctg aattttgcag ctgcagaatg tgtagtacct taaaaggttg 180 gcaacaatga gtaaaccaga attaaaggaa gacaagatgc tggaggttca ctttgtggga 240 gatgatgatg ttcttaatca cattctagat agagaaggag gagctaaatt gaagaaggag 300 cgagcgcagc ttttggtcaa ccccaaaaaa ataataaaga agccagaata tgatttggag 360 gaagatgacc aggaggtctt aaaagatcag aactatgtgg aaattatggg aagagatgtt 420 caagaatcat tgaaaaatgg ctctgctaca ggtggtggaa ataaagttta ttcttttcag 480 aatagaaaac actctgaaaa gatggctaaa ttagcttcag aactagcaaa aacaccacaa 540 aaaagtgttt cattcagttt gaagaatgat cctgagatta cgataaacgt tcctcaaagt 600 agcaagggcc attctgcttc agacaaggtt caaccgaaga acaatgacaa aagtgaattt 660 ctgtcaacag cacctcgtag tctaagaaaa agattaatag ttccaaggtc tcattctgac 720 agtgaaagcg aatattctgc ttccaactca gaggatgatg aaggggttgc acaggaacat 780 gaagaggaca ctaatgcagt catattcagc caaaagattc aagctcagaa tagagtagtt 840 tcagctcctg ttggcaaaga aacaccttct aagagaatga aaagagataa aacaagtgac 900 ttagtagaag aatattttga agctcacagc agttcaaaag ttttaacctc tgatagaaca 960 ctgcagaagc taaagagagc taaactggat cagcaaactt tgcgtaactt attgagcaag 1020 gtttcccctt ccttttctgc cgaacttaaa caactaaatc aacagtatga aaaattattt 1080 cataaatgga tgctgcaatt acaccttggg ttcaacattg tgctttatgg tttgggttct 1140 aagagagatt tactagaaag gtttcgaacc actatgctgc aagattccat tcacgttgtc 1200 atcaatggct tctttcctgg aatcagtgtg aaatcagtcc tgaattctat aacagaagaa 1260 gtcctcgatc atatgggtac tttccgcagt atactggatc agctagactg gatagtaaac 1320 aaatttaaag aagattcttc tttagaactc ttccttctca tccacaattt ggatagccag 1380 atgttgagag gagagaagag ccagcaaatc attggtcagt tgtcatcttt gcataacatt 1440 taccttatag catccattga ccacctcaat gctcctctca tgtgggatca tgcaaagcag 1500 agtcttttta actggctctg gtatgaaact actacataca gtccttatac tgaagaaacc 1560 tcctatgaga actctcttct ggtaaagcag tctggatccc tgccacttag ctcccttact 1620 catgtcttac gaagccttac ccctaatgca aggggaattt tcaggctact aataaaatac 1680 cagctggaca accaggataa cccttcttac attggccttt cttttcaaga tttttaccag 1740 cagtgtcggg aggcattcct cgtcaatagt gatctgacac tccgggccca gttaactgaa 1800 tttagggacc acaagcttat aagaacaaag aagggaactg atggagtaga gtatttatta 1860 attcctgttg ataatggaac attgactgat ttcttggaaa aggaagaaga ggaggcttga 1920 agctttcctt tattcttgaa tctcccatgg aagggttgta ccccagctgc cactcctcta 1980 gttgaaagtg ttgtgtttac atctgacatt aaattatttt tccagcatac aagatttaaa 2040 tttgggaagg gggggatgtc ctcaattaga actttttgat cagcctggct ggtaccgtct 2100 agtactatgc agcggtcctc aagttggaga aaatgtgcct ttcattcatt acctctctgg 2160 agacttcttg ctggaatgaa cagtgtgctc agggactatt tggaactgga tgtttttgaa 2220 ttattttata cttagagata ttctgaattt tttgagggcc ttttaacact ccccgagctg 2280 attgtttgca agtgtgtttg ttccagagtg tggaagtata aagacatggg catcacgtaa 2340 attggttttg tttgctattc tgtgtgtcag aaccaacgag tgtaatggag agggcaggtc 2400 atctcttatt gtttctaaaa caacttaaaa ggtgtagatt gggaagaggt gagtgatcca 2460 gctttctcct tttggattga ggctatgtac ttggtggggg caggggaggg aatatattat 2520 aatactattc agttgggata atgggaaaaa cagagtatat agggtatcta cccagcctag 2580 aaagcacagg aacaatacgt catatatttg gaacagttat tgtctgtgcc atgaccttca 2640 <210> SEQ ID NO 135 <211> LENGTH: 617 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/CAA85114.1 <309> DATABASE ENTRY DATE: 1997-08-11 <313> RELEVANT RESIDUES: (1)..(617) <400> SEQUENCE: 135 ccaatcaaag gattgaccca gagaacaaat caattttgaa tatgttatca gtgattgata 60 gaaaagaaca agaattgaaa gcaaaagaag aaaaacagca aagagaagct caggaacgtg 120 aaaacaagaa aattatgtta gagagcgcaa tgacgctgag aaacataact aacatcaaaa 180 ctcactctcc agtagagtta cttaatgagg gtaaaataag gctagaagac ccaatggatt 240 ttgaatctca attgatctat cccgcattaa ttatgtaccc cacgcaagat gaatttgatt 300 ttgtaggtga agtaagtgag ttaactactg tgcaagaact tgttgaccta gttttggaag 360 ggccgcaaga acgcttcaaa aaagaaggta aggaaaactt cacaccaaag aaagtgttgg 420 tgttcatgga aacaaaggca ggtggtttga ttaaagctgg taagaaactg acatttcacg 480 atatcttgaa gaaagagtcg ccagatgtac cattgttcga taacgctttg aaaatatata 540 ttgtgccaaa ggtagaaagt gaagggtgga tttccaagtg ggataagcaa aaagccttag 600 aaagaagatc tgtgtga 617 <210> SEQ ID NO 136 <211> LENGTH: 1173 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 136 atgtccaaaa tagagccagt cactgaaaaa gaagaagaat acgtttccga atgggataga 60 agaagatatg ttcccaaagc aggtgaacct gaattacctc cccaattatc agaattctct 120 aacaagacca cagacgaggt tattgaggaa ttgaatagat tgccattttt tatgacaaag 180 ttagatgaaa ctgatggaga tggcggagaa aatgtaaact tggaagcact taaaagtttg 240 gcatatgaag gtgatcctga cgaaattgcc tcaaatttca aaaatcaggg gaataattgt 300 tacaaattta aaaaatacaa agatgcaatt atattttata cgaaaggtct tgaagtaaac 360 tgtgacgtgg acgcaatcaa ttcagcatta tacttgaatc gtgctgcttg taacttggag 420 ttgaaaaatt accgtcggtg cattgaagat tgtaagaaag tattaatgct tgatgagaag 480 aatattaagg cttgtttccg ttcaggaaag gcattctttg caattgaaaa atacgatgaa 540 gcaatcaaag tgcttgaata cggtctaaat atagaaccag aaaacaaaga tttacagaaa 600 ttattacagc aagttcaaaa gaggcaagaa actttagctc aaataaaagc taaaaaggca 660 caagaagagg aacaagagcg gttgaaaaat atcgtgttgg agaattctat aaaattaaga 720 cacattgaaa tagtgaagtc ctcatctcct ccagaagtct tgaagactgc caagatacga 780 ttggaagacc ccaaagatta tcagtcacaa ttaatattcc ctgctatgat actatacccc 840 accaccgatg aatttgactt tattgcagaa ataagcgaat taactactcc tttggaattg 900 ctagagatgg tattaaatag acctagggaa tggtttgatg atccaaaaca caaggatttc 960 aatgtcaaaa aattggaatg ctttatggaa actgaatctg gtgggttgat taaagtgggc 1020 aagaaaattg aagttaacaa tgctttgatg aatgaaaaac ctaaggcacc attgtttgat 1080 aacgctttaa gactttatgt cgttccaaaa ttagacgtcg ccaaatggac atctgaatgg 1140 aataaagaaa ccgccttggc agctcgtaaa tag 1173 <210> SEQ ID NO 137 <211> LENGTH: 2005 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/NM_004623.1 <309> DATABASE ENTRY DATE: 2000-11-01 <313> RELEVANT RESIDUES: (1)..(2005) <400> SEQUENCE: 137 ctgggacccg ggctggaagg cagggcatca gctatggaac aacctgggca ggatcccacc 60 tcagacgacg tcatggactc gttcctggaa aagttccaga gccagcctta ccgtggcggc 120 tttcatgagg accagtggga gaaggaattt gaaaaggtcc ccctatttat gtcgagagcg 180 ccatcagaaa ttgatcccag ggagaatcct gacttggctt gtctccagtc aattattttt 240 gatgaggagc gttctccaga agaacaggcc aagacctata aagatgaggg caatgattac 300 tttaaagaaa aagactacaa gaaagctgta atttcataca ctgaaggctt aaagaagaaa 360 tgtgcagatc ctgatttgaa tgctgtcctt tataccaacc gggcagcagc acagtactat 420 ctgggcaatt ttcgttctgc tctcaatgat gtgacagctg ccagaaagct aaaaccctgc 480 cacctcaaag caataataag aggtgcctta tgccatctgg aactgataca ctttgccgag 540 gccgtgaact ggtgtgatga gggactgcaa atagatgcca aagagaagaa gcttctggaa 600 atgagggcta aagcagacaa gctgaagcga attgaacaga gggatgtgag gaaagccaac 660 ttgaaagaaa agaaggagag gaatcagaat gaggctttac tccaggccat caaggctagg 720 aatatcaggc tctcagaagc tgcctgtgag gatgaagatt cagcctcaga aggtctaggt 780 gagcttttcc tggatggact cagcactgag aacccccatg gagccaggct gagtctagat 840 ggccagggca ggctgagctg gcctgtgctc tttctgtacc cagagtatgc ccagtcggac 900 ttcatctctg cttttcatga ggactccagg tttattgatc atctaatggt gatgtttggt 960 gaaacacctt cttgggacct agagcaaaaa tattgcctga taatttggag gtctactttg 1020 aggatgagga cagggcagaa ctataccggg tgcctgccaa gagcaccttg ctacaggttc 1080 tacagcacca gaggtacttt gtaaaagccc tgacaccagc atttttggtc tgtgtaggat 1140 cctctccttt ttgcaagaat tttctccggg ggagaaaggt gtaccagata cgatgactaa 1200 gccagggccc ctggatctcc tcccttaccc tcctctgctg ggaacctagc acacctgaat 1260 cagctggaca tactgctgga gtccagtgct ttctttccgt caccctgggg atagtccttc 1320 ctggcatcgt ggtgggggag gagcctctgg cttccctaaa ctgcagctct ctggctggtc 1380 ttcactttcc tcagttgata taaaactctg gtcttggcca tgatgtcctt ggattccatc 1440 gctaaaggga ccatctgctg cagttaccac agcaactgac ttgagcggca cctggtctgt 1500 ggagatggac tcaggatcca gtgacatgat tctgaacttt tgtggagttt gacaccttag 1560 agaagctacc cctcaaactg cacatctaca cacaaacaaa caatgcatag gattccaagg 1620 ctttaaagct gagagaccct ggcctcaagt tatttcatgc gcacagaggg aagccatgtg 1680 gggttgctga agatgccttg aggtgaaatg ggggcaggaa agccacatct tgctctgcat 1740 ttataaagac cgtacaaact cagatccttg gtacccctaa aaagattgcc aattttcttc 1800 atctttgcca tatggaggac tgtgacagac tttggacagt ggcctcttga gttcctctgc 1860 agttttgaca tttaggattt tgtgtctttt aaactggaaa atcttctagc atgttgggtt 1920 gttacagagt atatttttgt ctgcagctgt ttgttgcccc attcctaaga ggagtttatc 1980 catcctgaaa aaaaaaaaaa aaaaa 2005 <210> SEQ ID NO 138 <211> LENGTH: 504 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/CAA98815.1 <309> DATABASE ENTRY DATE: 1997-08-11 <313> RELEVANT RESIDUES: (1)..(504) <400> SEQUENCE: 138 atgtctacta ttccctcaga aatcatcaat tggaccatct taaatgaaat tatatctatg 60 gatgacgatg attccgattt ttctaaaggt ctaattattc aatttatcga ccaggcacaa 120 acaacttttg ctcaaatgca acgacagctg gacggtgaaa aaaatcttac cgaattagac 180 aatctgggcc attttttaaa gggttcttct gctgcattag gcttacaaag aattgcctgg 240 gtttgtgaaa gaattcaaaa cttgggaaga aaaatggaac atttcttccc caacaagacc 300 gaattggtca acactctgag cgataaatcg attattaatg gaatcaatat tgatgaagat 360 gacgaggaaa taaagataca agtggacgat aaagacgaaa attccatata tctcatcttg 420 atagcaaaag ctttgaacca gtctaggttg gagttcaaac tggcgagaat tgagttatct 480 aaatattaca acacaaacct ataa 504 <210> SEQ ID NO 139 <211> LENGTH: 555 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 139 atgtcagaag ataaattaca aaaattacaa gactcaggac ttgtcgactg ggcagtgttt 60 agtgaaatag tgaccatgga cgaggatgaa gaagggtttt ccaaatcact agtagaagtc 120 tttgttagcc aagtggaaga aacatttgaa gaaattgata aatatttaaa ggaaaagaat 180 ttggagaaat tgtcatcgtc gggtcatttt ttgaaaggat ctgctgctgc tttggggttg 240 accaaaattt caaatcaatg cgaacgaatt caaaactatg gccataagat caactttgac 300 aattttcaat tggaagatat aaaaactaaa ggcgattcgg ccgtaagtgc ggaaaatgtg 360 gccgttaatg atggtgaaac taatccagaa aatggatcca atggcaacga aacaagtaat 420 aacaaaacaa atactagcaa tataccggat gaatcaagcg atgacttttg gatagcatta 480 attgaggatg cattagccaa ggcgagagat ggattcgacc aatctagaag agcattggac 540 gaatattacg aatag 555 <210> SEQ ID NO 140 <211> LENGTH: 7992 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/Z15005.1 <309> DATABASE ENTRY DATE: 1993-01-10 <313> RELEVANT RESIDUES: (1)..(7992) <400> SEQUENCE: 140 atggcggagg aaggagccgt ggccgtctgc gtgcgagtgc ggccgctgaa cagcagagaa 60 gaatcacttg gagaaactgc ccaagtttac tggaaaactg acaataatgt catttatcaa 120 gttgatggaa gtaaatcctt caattttgat cgtgtctttc atggtaatga aactaccaaa 180 aatgtgtatg aagaaatagc agcaccaatc atcgattctg ccatacaagg ctacaatggt 240 actatatttg cctatggaca gactgcttca ggaaaaacat ataccatgat gggttcagaa 300 gatcatttgg gagttatacc cagggcaatt catgacattt tccaaaaaat taagaagttt 360 cctgataggg aatttctctt acgtgtatct tacatggaaa tatacaatga aaccattaca 420 gatttactct gtggcactca aaaaatgaaa cctttaatta ttcgagaaga tgtcaatagg 480 aatgtgtatg ttgctgatct cacagaagaa gttgtatata catcagaaat ggctttgaaa 540 tggattacaa agggagaaaa gagcaggcat tatggagaaa caaaaatgaa tcaaagaagc 600 agtcgttctc ataccatctt taggatgatt ttggaaagca gagagaaggg tgaaccttct 660 aattgtgaag gatctgttaa ggtatcccat ttgaatttgg ttgatcttgc aggcagtgaa 720 agagctgctc aaacaggcgc tgcaggtgtg cggctcaagg aaggctgtaa tataaatcga 780 agcttattta ttttgggaca agtgatcaag aaacttagtg atggacaagt tggtggtttc 840 ataaattatc gagatagcaa gttaacacga attcttcaga attccttggg aggaaatcca 900 aagacacgta ttatctgcac aattactcca gtatcttttg atgaaactct tactgctctc 960 cagtttgcca gtactgctaa atatatgaag aatactcctt atgttaatga ggtatcaact 1020 gatgaagctc tcctgaaaag gtatagaaaa gaaataatgg atcttaaaaa acaattagag 1080 gaggtttctt tagagacgcg ggctcaggca atggaaaaag accaattggc ccaacttttg 1140 gaagaaaaag atttgcttca gaaagtacag aatgagaaaa ttgaaaactt aacacggatg 1200 ctggtgacct cttcttccct cacgttgcaa caggaattaa aggctaaaag aaaacgaaga 1260 gttacttggt gccttggcaa aattaacaaa atgaagaact caaactatgc agatcaattt 1320 aatataccaa caaatataac aacaaaaaca cataagcttt ctataaattt attacgagaa 1380 attgatgaat ctgtctgttc agagtctgat gttttcagta acactcttga tacattaagt 1440 gagatagaat ggaatccagc aacaaagcta ctaaatcagg agaatataga aagtgagttg 1500 aactcacttc gtgctgacta tgataatctg gtattagact atgaacaact acgaacagaa 1560 aaagaagaaa tggaattgaa attaaaagaa aagaatgatt tggatgaatt tgaggctcta 1620 gaaagaaaaa ctaaaaaaga tcaagagatg caactaattc atgaaatttc gaacttaaag 1680 aatttagtta agcatcgaga agtatataat caagatcttg agaatgaact cagttcaaaa 1740 gtagagctgc ttagagaaaa ggaagaccag attaagaagc tacaggaata catagactct 1800 caaaagctag aaaatataaa aatggacttg tcatactcat tggaaagcat tgaagaccca 1860 aaacaaatga agcagactct gtttgatgct gaaactgtag cccttgatgc caagagagaa 1920 tcagcctttc ttagaagtga aaatctggag ttgaaggaga aaatgaaaga acttgcaact 1980 acatacaagc aaatggaaaa tgatattcag ttatatcaaa gccaattgga ggcaaaaaag 2040 aaaatgcaag ttgatctgga gaaagaatta caatctgctt ttaatgagat aacaaaactc 2100 acctccctta tagatggcaa agttccaaaa gatttgctct gtaatttgga attggaagga 2160 aagattactg atcttcagaa agaactaaat aaagaagttg aagaaaatga agctttgcgg 2220 gaagaagtca ttttgctttc agaattgaaa tctttacctt ctgaagtaga aaggctgagg 2280 aaagagatac aagacaaatc tgaagagctc catataataa catcagaaaa agataaattg 2340 ttttctgaag tagttcataa ggagagtaga gttcaaggtt tacttgaaga aattgggaaa 2400 acaaaagatg acctagcaac tacacagtcg aattataaaa gcactgatca agaattccaa 2460 aatttcaaaa cccttcatat ggactttgag caaaagtata agatggtcct tgaggagaat 2520 gagagaatga atcaggaaat agttaatctc tctaaagaag cccaaaaatt tgattcgagt 2580 ttgggtgctt tgaagaccga gctttcttac aagacccaag aacttcagga gaaaacacgt 2640 gaggttcaag aaagactaaa tgagatggaa cagctgaagg aacaattaga aaatagagat 2700 tctccgctgc aaactgtaga aagggagaaa acactgatta ctgagaaact gcagcaaact 2760 ttagaagaag taaaaacttt aactcaagaa aaagatgatc taaaacaact ccaagaaagc 2820 ttgcaaattg agagggacca actcaaaagt gatattcacg atactgttaa catgaatata 2880 gatactcaag aacaattacg aaatgctctt gagtctctga aacaacatca agaaacaatt 2940 aatacactaa aatcgaaaat ttctgaggaa gtttccagga atttgcatat ggaggaaaat 3000 acaggagaaa ctaaagatga atttcagcaa aagatggttg gcatagataa aaaacaggat 3060 ttggaagcta aaaataccca aacactaact gcagatgtta aggataatga gataattgag 3120 caacaaagga agatattttc tttaatacag gagaaaaatg aactccaaca aatgttagag 3180 agtgttatag cagaaaagga acaattgaag actgacctaa aggaaaatat tgaaatgacc 3240 attgaaaacc aggaagaatt aagacttctt ggggatgaac ttaaaaagca acaagagata 3300 gttgcacaag aaaagaacca tgccataaag aaagaaggag agctttctag gacctgtgac 3360 agactggcag aagttgaaga aaaactaaag gaaaagagcc agcaactcca agaaaaacag 3420 caacaacttc ttaatgtaca agaagagatg agtgagatgc agaaaaagat taatgaaata 3480 gagaatttaa agaatgaatt aaagaacaaa gaattgacat tggaacatat ggaaacagag 3540 aggcttgagt tggctcagaa acttaatgaa aattatgagg aagtgaaatc tataaccaaa 3600 gaaagaaaag ttctaaagga attacagaag tcatttgaaa cagagagaga ccaccttaga 3660 ggatatataa gagaaattga agctacaggc ctacaaacca aagaagaact aaaaattgct 3720 catattcacc taaaagaaca ccaagaaact attgatgaac taagaagaag cgtatctgag 3780 aagacagctc aaataataaa tactcaggac ttagaaaaat cccataccaa attacaagaa 3840 gagatcccag tgcttcatga ggaacaagag ttactgccta atgtgaaaaa agtcagtgag 3900 actcaggaaa caatgaatga actggagtta ttaacagaac agtccacaac caaggactca 3960 acaacactgg caagaataga aatggaaagg ctcaggttga atgaaaaatt tcaagaaagt 4020 caggaagaga taaaatctct aaccaaggaa agagacaacc ttaaaacgat aaaagaagcc 4080 cttgaagtta aacatgacca gctgaaagaa catattagag aaactttggc taaaatccag 4140 gagtctcaaa gcaaacaaga acagtcctta aatatgaaag aaaaagacaa tgaaactacc 4200 aaaatcgtga gtgagatgga gcaattcaaa cccaaagatt cagcactact aaggatagaa 4260 atagaaatgc tcggattgtc caaaagactt caagaaagtc atgatgaaat gaaatctgta 4320 gctaaggaga aagatgacct acagaggctg caagaagttc ttcaatctga aagtgaccag 4380 ctcaaagaaa acataaaaga aattgtagct aaacacctgg aaactgaaga ggaacttaaa 4440 gttgctcatt gttgcctgaa agaacaagag gaaactatta atgagttaag agtgaatctt 4500 tcagagaagg aaactgaaat atcaaccatt caaaagcagt tagaagcaat caatgataaa 4560 ttacagaaca agatccaaga gatttatgag aaagaggaac aacttaatat aaaacaaatt 4620 agtgaggttc aggaaaacgt gaatgaactg aaacaattca aggagcatcg caaagccaag 4680 gattcagcac tacaaagtat agaaagtaag atgctcgagt tgaccaacag acttcaagaa 4740 agtcaagaag aaatacaaat tatgattaag gaaaaagagg aaatgaaaag agtacaggag 4800 gcccttcaga tagagagaga ccaactgaaa gaaaacacta aagaaattgt agctaaaatg 4860 aaagaatctc aagaaaaaga atatcagttt cttaagatga cagctgtcaa tgagactcag 4920 gagaaaatgt gtgaaataga acacttgaag gagcaatttg agacccagaa gttaaacctg 4980 gaaaacatag aaacggagaa tataaggttg actcagatac tacatgaaaa ccttgaagaa 5040 atgagatctg taacaaaaga aagagatgac cttaggagtg tggaggagac tctcaaagta 5100 gagagagacc agctcaagga aaaccttaga gaaactataa ctagagacct agaaaaacaa 5160 gaggagctaa aaattgttca catgcatctg aaggagcacc aagaaactat tgataaacta 5220 agagggattg tttcagagaa aacaaatgaa atatcaaata tgcaaaagga cttagaacac 5280 tcaaatgatg ccttaaaagc acaggatctg aaaatacaag aggaactaag aattgctcac 5340 atgcatctga aagagcagca ggaaactatt gacaaactca gaggaattgt ttctgagaag 5400 acagataaac tatcaaatat gcaaaaagat ttagaaaatt caaatgctaa attacaagaa 5460 aagattcaag aacttaaggc aaatgaacat caacttatta cgttaaaaaa agatgtcaat 5520 gagacacaga aaaaagtgtc tgaaatggag caactaaaga aacaaataaa agaccaaagc 5580 ttaactctga gtaaattaga aatagagaat ttaaatttgg ctcaagaact tcatgaaaac 5640 cttgaagaaa tgaaatctgt aatgaaagaa agagataatc taagaagagt agaggagaca 5700 ctcaaactgg agagagacca actcaaggaa agcctgcaag aaaccaaagc tagagatctg 5760 gaaatacaac aggaactaaa aactgctcgt atgctatcaa aagaacacaa agaaactgtt 5820 gataaactta gagaaaaaat ttcagaaaag acaattcaaa tttcagacat tcaaaaggat 5880 ttagataaat caaaagatga attacagaaa aagatccaag aacttcagaa aaaagaactt 5940 caactgctta gagtgaaaga agatgtcaat atgagtcata aaaaaattaa tgaaatggaa 6000 cagttgaaga agcaatttga gccaaactat ctatgcaagt gtgagatgga taacttccag 6060 ttgactaaga aacttcatga aagccttgaa gaaataagaa ttgtagctaa agaaagagat 6120 gagctaagga ggataaaaga atctctcaaa atggaaaggg accaattcat agcaacctta 6180 agggaaatga tagctagaga ccgacagaac caccaagtaa aacctgaaaa aaggttacta 6240 agtgatggac aacagcacct tatggaaagc ctgagagaaa agtgctctag aataaaagag 6300 cttttgaaga gatactcaga gatggatgat cattatgagt gcttgaatag attgtctctt 6360 gacttggaga aggaaattga attccacaga atcatgaaga aactgaagta tgtgttaagc 6420 tatgttacaa aaataaaaga agaacaacat gaatgcatca ataaatttga aatggatttt 6480 attgatgaag tggaaaagca aaaggaattg ctaattaaaa tacagcacct tcaacaagat 6540 tgtgatgtac catccagaga attaagggat ctcaaattga accagaatat ggatctacat 6600 attgaggaaa ttctcaaaga tttctcagaa agtgagttcc ctagcataaa gactgaattt 6660 caacaagtac taagtaatag gaaagaaatg acacagtttt tggaagagtg gttaaatact 6720 cgttttgata tagaaaagct taaaaatggc atccagaaag aaaatgatag gatttgtcaa 6780 gtgaataact tctttaataa cagaataatt gccataatga atgaatcaac agagtttgag 6840 gaaagaagtg ctaccatatc caaagagtgg gaacaggacc tgaaatcact gaaagagaaa 6900 aatgaaaaac tatttaaaaa ctaccaaaca ttgaagactt ccttggcatc tggtgcccag 6960 gttaatccta ccacacaaga caataagaat cctcatgtta catcaagagc tacacagtta 7020 accacagaga aaattcgaga gctggaaaat tcactgcatg aagctaaaga aagtgctatg 7080 cataaggaaa gcaagattat aaagatgcag aaagaacttg aggtgactaa tgacataata 7140 gcaaaacttc aagccaaagt tcatgaatca aataaatgcc ttgaaaaaac aaaagagaca 7200 attcaagtac ttcaggacaa agttgcttta ggagctaagc catataaaga agaaattgaa 7260 gatctcaaaa tgaagcttgt gaaaatagac ctagagaaaa tgaaaaatgc caaagaattt 7320 gaaaaggaaa tcagtgctac aaaagccact gtagaatatc aaaaggaagt tataaggcta 7380 ttgagagaaa atctcagaag aagtcaacag gcccaagata cctcagtgat atcagaacat 7440 actgatcctc agccttcaaa taaaccctta acttgtggag gtggcagcgg cattgtacaa 7500 aacacaaaag ctcttatttt gaaaagtgaa catataaggc tagaaaaaga aatttctaag 7560 ttaaagcagc aaaatgaaca gctaataaaa caaaagaatg aattgttaag caataatcag 7620 catctttcca atgaggtcaa aacttggaag gaaagaaccc ttaaaagaga ggctcacaaa 7680 caagtaactt gtgagaattc tccaaagtct cctaaagtga ctggaacagc ttctaaaaag 7740 aaacaaatta caccctctca atgcaaggaa cggaatttac aagatcctgt gccaaaggaa 7800 tcaccaaaat cttgtttttt tgatagccga tcaaagtctt taccatcacc tcatccagtt 7860 cgctattttg ataactcaag tttaggcctt tgtccagagg tgcaaaatgc aggagcagag 7920 agtgtggatt ctcagccagg tccttggcac gcctcctcag gcaaggatgt gcctgagtgc 7980 aaaactcagt ag 7992 <210> SEQ ID NO 141 <211> LENGTH: 282 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/AAB68435.1 <309> DATABASE ENTRY DATE: 1997-09-03 <313> RELEVANT RESIDUES: (1)..(282) <400> SEQUENCE: 141 atgtctttct taggtttcgg tggtggtcag cctcaattat catctcaaca aaagattcaa 60 gctgcggaag ctgaactaga tttggtcaca gacatgttca ataaattggt taataactgt 120 tataaaaaat gtatcaatac ttcttattcc gagggtgagc tgaataagaa tgaatcttcg 180 tgcctagaca gatgtgtggc caaatatttt gagaccaatg ttcaagtcgg tgaaaacatg 240 cagaaaatgg gccaatcatt taacgcagcc ggtaagtttt ag 282 <210> SEQ ID NO 142 <211> LENGTH: 278 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 142 atgtttggct taggtggtac tactcctcaa atttcatctc aacaaaaact tcaagctgct 60 gaagctgaat tagatatggt tactggcatg ttcaatgctt tagtttccca atgtcacacc 120 aaatgtatca acaaatcata taatgaagct gatatttcaa agcaagaatc tttatgtctt 180 gatagatgtg ttgccaaata ttttgaaacc aatgttcaag ttggtgaaaa tatgcaaaaa 240 ttaggtcaat ctggtcaatt tatgggtaga agataaat 278 <210> SEQ ID NO 143 <211> LENGTH: 658 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/NM_012456.1 <309> DATABASE ENTRY DATE: 2001-12-19 <313> RELEVANT RESIDUES: (1)..(658) <400> SEQUENCE: 143 ggagcctcac grgagcgkgg taacgttata gtatttgtca gaagttgggg tctccgtggg 60 cattgtgatc cgtcccaggc agtggattag gaggccagaa ggagatccct tccacggtgc 120 taggctgaga tggatcctct cagggcccaa cagctggctg cggagctgga ggtggagatg 180 atggccgata tgtacaacag aatgaccagt gcctgccacc ggaagtgtgt gcctcctcac 240 tacaaggaag cagagctctc caagggcgag tctgtgtgcc tggaccgatg tgtctctaag 300 tacctggaca tccatgagcg gatgggcaaa aagttgacag agttgtctat gcaggatgaa 360 gagctgatga agagggtgca gcagagctct gggcctgcat gaggtccctg tcagtataca 420 ccctggggtg taccccaccc cttcccactt taataaacgt gctccctgtt gggtgtcatc 480 tgtgaagact gccaggccta ggctctctgt agagagtctt caagatcccg gagtggtagc 540 gctgtctcct ggtgaaggag tatttgtcac actggaatgt gactgtgtgt gtatgtatgt 600 gtatatatat atatatatat atatataaac aagtttgttg acacctacaa aaaaaaaa 658 <210> SEQ ID NO 144 <211> LENGTH: 1980 <212> TYPE: DNA <213> ORGANISM: Saccharomyces cerevisiae <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Genbank/AAB64555.1 <309> DATABASE ENTRY DATE: 2000-10-10 <313> RELEVANT RESIDUES: (1)..(1980) <400> SEQUENCE: 144 atgacaacgg aagatccaga ttcaaatcac ttaagttccg aaactggcat taaattggca 60 ttggacccga acttaattac attggcacta agttctaatc caaactctag ccttcattca 120 ccaacgtctg atgaacccgt acctgaatct gcaggaaaag cagatactag tattcgacta 180 gaaggtgatg agttagagaa taaaactaag aaagacaatg ataagaactt aaaatttttg 240 aagaataaag attctctagt cagtaatcca cacgaaattt atggctccat gccgttggag 300 caattgatcc caatcatctt aagacagcgt ggtccaggct ttaaattcgt tgatttaaat 360 gaaaaagaat tgcaaaatga gattaagcag cttggtagtg atagtagtga cggtcataac 420 agcgagaaga aggacactga tggcgctgat gagaatgtac aaattggaga agatttcatg 480 gaagtggatt atgaagataa agataatcca gtggattcac gaaatgaaac agaccacaaa 540 acgaatgaaa atggcgagac cgatgataat attgaaacgg taatgacaca ggaacagttt 600 gttaaaagaa ggagggatat gctagagcat ataaatctgg ccatgaacga atcgtctttg 660 gctttggaat tcgtttcttt gctactgtcg agtgttaaag agtctacagg tatgtcatca 720 atgtcaccat ttcttaggaa agttgttaaa ccttctagtt taaacagtga taaaattcca 780 tatgttgcac ctacaaaaaa agaatatatc gagttggata tattgaataa gggatggaag 840 ttacaaagtt taaacgaatc taaagatctc ctacgcgcaa gttttaataa actgagttcc 900 atattacaga acgaacatga ctattggaat aagataatgc agagtattag caacaaggat 960 gttattttta agattaggga caggactagt ggtcaaaagc tgttggcaat taagtatggt 1020 tacgaagact ctggatctac ctataagcat gacagaggta ttgctaatat aaggaataat 1080 atagaatcac aaaatttgga tttgataccc cacagtagtt cagtgttcaa aggcactgat 1140 ttcgtacatt cagtaaagaa attcttaagg gttcgtatct tcacaaaaat cgaatcagaa 1200 gatgattaca tattgagtgg cgaaagtgtg atggataggg atagtgaaag tgaagaagct 1260 gaaacgaaag atatcagaaa gcaaatccaa cttttgaaaa agatcatttt tgaaaaagaa 1320 ctgatgtacc aaataaagaa agaatgcgct ttgttgattt cctatggtgt cagtattgaa 1380 aacgaaaaca aggtaataat tgaactacct aacgaaaaat ttgaaatcga gttgttgtcc 1440 cttgacgatg actccattgt caatcatgaa caagacttac caaaaatcaa cgacaagaga 1500 gcaaatttaa tgcttgttat gttgagacta ttattagtcg ttatattcaa gaaaacatta 1560 cgatcgagaa taagctcacc ccacggactg atcaatttga atgttgacga tgatatctta 1620 ataatacgtc ccattcttgg taaagttcgg tttgctaatt acaaactgtt actaaaaaaa 1680 atcataaagg attacgtgct cgatatagtt cctggctcaa gtataacaga aacggaagtt 1740 gagagagaac aacctcaaga aaataaaaac attgatgatg aaaatataac taaattaaat 1800 aaagagatcc gtgccttcga taaactattg aatataccta gacgtgaact caaaataaat 1860 ctaccattaa ctgagcacaa aagccctaat ctaagtttaa tgctcgaaag tcctaactat 1920 tgtaacgcac tcattcacat caagttttca gctggtacgg aagccaacgc agtgtccttt 1980 <210> SEQ ID NO 145 <211> LENGTH: 1849 <212> TYPE: DNA <213> ORGANISM: Candida albicans <400> SEQUENCE: 145 atggtggaaa aacagtttaa catagaccta gagttaaatg atactggtca tatagatcca 60 ttcttacaag atgagtatgt ttgctttcta actttattgg tatttttggt tctgtttttt 120 agtttactaa ccttgaccaa gagataaatt gaaacttgag gaactaattc cacgaatttt 180 atttgaacgt aaatcatttt tgaatgtgac ggaggattct ttgagaaaag aaatagacaa 240 ttcattgaag atttccgaag aggatgcttt agacactgaa gaaagtagag aggacacagt 300 tgaagcagat caacaagaag tgttcaataa acacaagttt gaattatcga aaaatataaa 360 caatgcactt aatgaaaccc aactttcctt agattttgta tccttattaa tatcttcagt 420 gaaaccaagt ttggcaaaat ctaccatttc accacacttg tcaaaatttg tcaaaccgac 480 atctttaaat tcggatagat tgggtcaaga tagtaatgat aatcaagaga gtaaggctac 540 tgattctttt ggacaaggat ggaaattgga gtcacttgga aagataaccg atcttttcag 600 agaagctagt actaatttaa acgatcaagt tatcaaagaa agacgatatt ggaatatgat 660 aaatttggtg cttgccaacg acgaggttct atttcgaatg agggaccccc aaaataatgc 720 tagagcaata ggagtgaaat atgggtatgg agattcagga tcaaattttc acgaccaagg 780 gttggcattg ttacgcaagg acaaccaaac aggagaaatc tcatttcacc ccatatcgtc 840 aatcaacaat gctaaaattg tagaaaaagt ttcgagattt attagagtga aaattttgag 900 ccaaatagat ggggactata tgcttacagg acagtcaatt tttaattttg attttgaaaa 960 aagcaagcaa agcataatta atgacatcga aaaggctaga ttctttttat ttgaggagga 1020 cttgtttcat caattgatac gcgaggccaa attgttggta aactacaatg tgtcaatcat 1080 atcgaataaa ataataattg aaatcaacaa cattattatt gaaatagagt ctatcgtgta 1140 tgatgagttg aatgaggagg aactagaaaa ctattaccag aatgtaaatg aatattccac 1200 cttacacaat aaaaagtgtc agcttatttt aaactacttg aaacttatgc tttgttgtta 1260 ttacaaatac aatctcaaat tgaaacagaa ggttccaaca gcattgacta aatggaagca 1320 gagtaactcc catcctttga ttttgcgtcc gttagtgggt aatatgaggc atgagttaaa 1380 tttgctaaat atgaagagtg ttttagatcg attaatgcac gctcatgaga gtgaactttc 1440 ttattccaaa ctagatgtgg agaagtttat taacttagcc acaagaagca aaaagcaaaa 1500 cccattccaa aagtcaattg aaaagccaat ttcaaagttc catttagttt tatgcaacaa 1560 aacctctaat atgttggacg tcaacataca attgacaact aatgagctgt ttgtcaatct 1620 aatcatcaat atgacaatta ttagatttga aacagaagac gattttaaga acaatgtcaa 1680 tggtattaac gttctacagc ttgggttcag tgatttcaat gaaatcgaag aatgcttgga 1740 ttggtcgatc caaaattttg tataggacac aacattttct gattttaaag aagtagagga 1800 cttcctacat tttattgtcg ctgagtacat ccagcaaaag aaggtgtaa 1849 <210> SEQ ID NO 146 <211> LENGTH: 2760 <212> TYPE: DNA <213> ORGANISM: Homo sapiens <300> PUBLICATION INFORMATION: <308> DATABASE ACCESSION NUMBER: Human Genbank/AB015617.1 <309> DATABASE ENTRY DATE: 2000-01-06 <313> RELEVANT RESIDUES: (1)..(2760) <400> SEQUENCE: 146 atgtatggaa gtgcccgctc tgttgggaag gtggagccga gcagccagag ccctgggcgt 60 tcacccaggc ttccacgttc ccctcgcttg ggtcaccgtc gaaccaacag tacgggaggg 120 agttcgggaa gcagtgttgg aggtggcagt gggaaaaccc tttcaatgga aaatatacaa 180 tctttaaatg ctgcctatgc cacctctggc cctatgtatc taagtgacca tgaaaatgtg 240 ggttcagaaa cacctaaaag caccatgaca cttggccgtt ctgggggacg tctgccttac 300 ggtgttcgga tgactgctat gggtagtagc cccaatatag ctagcagtgg ggttgctagt 360 gacaccatag catttggaga gcatcacctc cctcctgtga gtatggcatc cactgtacct 420 cactcccttc gtcaggcgag agataacaca atcatggatc tgcagacaca gctgaaggaa 480 gtattaagag aaaatgatct cttgcggaag gatgtggaag taaaggagag caaattgagt 540 tcttcaatga atagcatcaa gaccttctgg agcccagagc tgaagaagga acgagccctg 600 agaaaagatg aagcttccaa aatcaccatt tggaaggaac agtacagagt tgtacaggag 660 gaaaaccagc acatgcagat gacaatccag gctctccagg atgaattgcg gatccagagg 720 gacctgaatc agctgtttca gcaggatagt agcagcagga ctggcgaacc ttgtgtagca 780 gagctgacag aggagaactt tcagaggctt catgctgagc atgagcggca ggccaaagag 840 ctgtttcttc ttcgaaagac attggaggaa atggagctgc gtattgagac tcaaaagcag 900 accctaaatg ctcgggatga atccattaag aagcttctgg aaatgttgca gagcaaagga 960 ctttctgcca aggctaccga ggaagaccat gagagaacaa gacgactggc agaggcagag 1020 atgcacgttc atcacctaga aagccttttg gagcagaagg aaaaagagaa cagtatgttg 1080 agagaggaga tgcatcgaag gtttgagaat gctcctgatt ctgccaaaac aaaagctctg 1140 caaactgtta ttgagatgaa ggattcaaaa atttcctcta tggagcgtgg gcttcgagac 1200 ctggaagagg aaattcagat gctgaaatcg aatggtgctt tgagtactga ggaaagggaa 1260 gaagaaatga agcaaatgga agtgtatcgg agccattcta aatttatgaa aaataagatt 1320 ggccaggtga aacaggagct gtccagaaag gacacagaac tactcgccct gcagacaaag 1380 ctagaaacac tcacaaacca gttctcagat agtaaacagc acattgaagt gttgaaggag 1440 tccttgactg ctaaggagca gagggctgcc atcctgcaga ctgaggtgga tgctctccga 1500 ttgcgtttgg aagagaagga aaccatgttg aataaaaaga caaaacaaat tcaggatatg 1560 gctgaagaga aggggacaca agctggagag atacatgacc tcaaggacat gttggatgtg 1620 aaggagcgga aggttaatgt tcttcagaag aagattgaaa atcttcaaga gcagcttaga 1680 gacaaggaaa agcagatgag cagcttgaaa gaacgggtca aatccttgca ggctgacacc 1740 accaacactg acactgcctt gacaactttg gaggaggccc ttgcagagaa agagcggaca 1800 attgaacgct taaaggagca gagggacaga gatgagcgag agaagcaaga ggaaattgat 1860 aactacaaaa aagatcttaa agacttgaag gaaaaagtca gcctgttgca aggcgacctt 1920 tcagagaaag aggcttcact tttggatctg aaagagcatg cttcttctct ggcatcctca 1980 ggactgaaaa aggactcacg gcttaagaca ctagagattg ctttggagca gaagaaggag 2040 gagtgtctga aaatggaatc acaattgaaa aaggcacatg aggcagcatt ggaagccaga 2100 gccagtccag agatgagtga ccgaatacag cacttggaga gagagatcac caggtacaaa 2160 gatgaatcta gcaaggccca ggcagaagtt gatcgactct tagaaatctt gaaggaggtg 2220 gaaaatgaga agaatgacaa agataagaag atagctgagt tggaaagtct cacctcaagg 2280 caagtgaaag accagaataa gaaggtagca aatctgaagc acaaggaaca ggtggaaaaa 2340 aagaagagtg cacaaatgtt agaggaggcg cgacgacggg aggacaatct caacgacagc 2400 tctcagcagc tacaggtgga ggagttactg atggccatgg agaaggtaaa gcaggaacta 2460 gaatccatga aagcaaagct gtcctccacc cagcagtctc tggcagaaaa ggaaactcac 2520 ttgactaatc ttcgggcaga gagaaggaaa cacttagagg aagttctgga gatgaagcaa 2580 gaagctcttc tggctgccat tagtgaaaaa gacgccaata tagctctctt ggagctttcg 2640 tcctctaaga agaagaccca agaggaagtg gctgccctga agcgggagaa ggatcgtctg 2700 gtacagcagc ttaagcagca gacgcaaaat cgaatgaagc taatggccga caactacgag 2760 

We claim:
 1. A method of screening or testing a candidate anti-fungal compound for interaction with an essential protein, comprising; a) providing an essential protein selected from the group consisting of RPC34, POP3, TFA2, NAB2, MPT1, MTR2, BOS1, POL30, YMR131C, SQT1, MTW1, TFB1, SPC98, BFR2, RNA1, GCD7, SKI6, NIP1, LCP5, NCE103, ECO1, ORC2, CNS1, YPD1, TIM10 and SRB4; b) providing one or more test compounds; c) contacting said essential protein with said one or more test compounds; and d) determining the interaction of the test compound with said essential protein.
 2. The method of claim 1, wherein said essential protein comprises a fragment, a function-conservative variant, a fragment or an active fragment of the essential protein.
 3. A method of screening or testing a candidate anti-fungal compound for modulation of activity of an essential protein, comprising; a) providing an essential protein selected from the group consisting of RPC34, POP3, TFA2, NAB2, MPT1, MTR2, BOS1, POL30, YMR131C, SQT1, MTW1, TFB1, SPC98, BFR2, RNA1, GCD7, SKI6, NIP1, LCP5, NCE103, ECO1, ORC2, CNS1, YPD1, TIM10 and SRB4; b) providing one or more test compounds; c) contacting said essential protein with said one or more test compounds;and d) determining the modulation of activity of said essential protein in the presence of said test compound.
 4. The method of claim 3, wherein said essential protein comprises a fragment, a function-conservative variant, a fragment or an active fragment of the essential protein.
 5. A method of screening or testing a candidate anti-fungal compound for interaction with an essential protein in a culture of cells, comprising; a) providing an essential protein within a culture of cells that express said essential protein is selected from the group consisting of RPC34, POP3, TFA2, NAB2, MPT1, MTR2, BOS1, POL30, YMR131C, SQT1, MTW1, TFB1, SPC98, BFR2, RNA1, GCD7, SKI6, NIP1, LCP5, NCE103, ECO1, ORC2, CNS1, YPD1, TIM10 and SRB4; b) providing one or more test compounds; c) contacting said culture of cells with said one or more test compounds;and d) determining the interaction said test compound with said essential protein.
 6. The method of claim 5, wherein said culture of cells comprises bacterial cells, fungal cells, yeast cells or mammalian cells.
 7. The method of claim 5, wherein said culture of cells comprises recombinant cells.
 8. The method of claim 5, wherein when expression or function of said essential protein is reduced or blocked, growth rate of a fungus expressing said essential protein is inhibited.
 9. The method of claim 5, wherein when expression or function of said essential protein is reduced or blocked, viability of a fungus expressing said essential protein becomes reduced.
 10. The method of claim 5, wherein said essential protein comprises a fragment, a function-conservative variant, a fragment or an active fragment of the essential protein.
 11. A method of screening or testing a candidate anti-fungal compound for effects on growth or viability of a culture of cells, comprising; a) providing an essential protein within a culture of cells that express an essential protein selected from the group consisting of RPC34, POP3, TFA2, NAB2, MPT1, MTR2, BOS1, POL30, YMR131C, SQT1, MTW1, TFB1, SPC98, BFR2, RNA1, GCD7, SKI6, NIP1, LCP5, NCE103, ECO1, ORC2, CNS1, YPD1, TIM10 and SRB4; b) providing one or more test compounds; c) contacting said culture of cells with said one or more test compounds;and d) determining the effects on the growth or viability of said culture of cells.
 12. The method of claim 11, wherein said culture of cells comprises fungal cells or yeast cells.
 13. The method of claim 11, wherein said culture of cells comprises recombinant cells.
 14. The method of claim 11, wherein when expression or function of said essential protein is reduced or blocked,the growth rate of a fungus expressing said essential protein is inhibited.
 15. The method of claim 11, wherein when expression or function of said essential protein is reduced or blocked.viability of a fungus expressing said essential protein is reduced.
 16. The method of claim 11, wherein said essential protein comprises a fragment, a function-conservative variant, a fragment or an active fragment of said essential protein.
 17. A method of screening or testing a candidate anti-fungal compound for interaction with an essential protein in a non-human animal, comprising; a) providing a non-human animal with a cell or group of cells expressing an essential protein selected from the group consisting of RPC34, POP3, TFA2, NAB2, MPT1, MTR2, BOS1, POL30, YMR131C, SQT1, MTW1, TFB1, SPC98, BFR2, RNA1, GCD7, SKI6, NIP1, LCP5, NCE103, ECO1, ORC2, CNS1, YPD1, TIM10 and SRB4; b) providing one or more test compounds; c) contacting said non-human animal with said one or more test compounds;and d) determining the interaction of said test compound with said essential protein.
 18. The method of claim 17, wherein when the interaction of said test compound with said essential protein reduces or blocks expression or function of said essential growth rate of a fungus expressing said essential protein is inhibited.
 19. The method of claim 17, wherein when the interaction of said test compound with said essential protein reduces or blocks expression or function of said essential, viability of a fungus expressing said essential protein is reduced.
 20. The method of claim 17, wherein said essential protein comprises a fragment, a function-conservative variant, a fragment or an active fragment of the essential protein.
 21. A method of screening or testing the effects of a candidate anti-fungal compound on growth or viability of a cell or group of cells expressing an essential protein in a non-human animal, comprising; a) providing the non-human animal with the cell or group of cells expressing an essential protein selected from the group consisting of RPC34, POP3, TFA2, NAB2, MPT1, MTR2, BOS1, POL30, YMR131C, SQT1, MTW1, TFB1, SPC98, BFR2, RNA1, GCD7, SKI6, NIP1, LCP5, NCE103, ECO1, ORC2, CNS1, YPD1, TIM10 and SRB4; b) providing one or more test compounds; c) contacting said test animal with said one or more test compounds;and d) determining the effects on the growth or viability of said cell or group of cells.
 22. The method of claim 21, wherein when expression or function of said essential protein is reduced or blocked growth rate of a fungus expressing said essential protein is inhibited.
 23. The method of claim 21, wherein when expression or function of said essential protein is reduced or blocked, viability of a fungus expressing said essential protein becomes reduced.
 24. The method of claim 21, wherein said essential protein comprises a fragment, a function-conservative variant, a fragment or an active fragment of said essential protein.
 25. The method of claim 3, wherein the modulation of activity comprises modulation of fungal gene transcription.
 26. The method of claim 5, wherein the interaction is assessed by binding of said test compound with said essential protein or activity of said essential protein in the presence of said test compound.
 27. The method of claim 17, wherein the interaction is assessed by binding of said test compound with said essential protein or activity of said essential protein in the presence of said test compound.
 28. A method of screening or testing a candidate anti-fungal compound for binding with an essential protein, comprising; a) providing an essential protein selected from the group consisting of RPC34, POP3, TFA2, NAB2, MPT1, MTR2, BOS1, POL30, YMR131C, SQT1, MTW1, TFB1, SPC98, BFR2, RNA1, GCD7, SKI6, NIP1, LCP5, NCE103, ECO1, ORC2, CNS1, YPD1, TIM10 and SRB4; b) providing one or more test compounds; c) contacting said essential protein with said one or more test compounds;and d) determining the binding of the test compound with said essential protein.
 29. A method of screening or testing a candidate anti-fungal compound for modulation transcription of a gene encoding an essential protein, comprising; a) providing a gene encoding an essential protein selected from the group consisting of RPC34, POP3, TFA2, NAB2, MPT1, MTR2, BOS1, POL30, YMR131C, SQT1, MTW1, TFB1, SPC98, BFR2, RNA1, GCD7, SKI6, NIP1, LCP5, NCE103, ECO1, ORC2, CNS1, YPD1, TIM10 and SRB4; b) providing one or more test compounds; c) contacting said gene with said one or more test compounds; and d) determining the modulation of transcription of said gene of said essential protein in the presence of said test compound 